Alkine (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Alkine" in German language version.

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  • Jaime Wisniak: Edmond Davy. In: Educación Química. Band 31, Nr. 4, 6. Oktober 2020, S. 144, doi:10.22201/fq.18708404e.2020.4.72934.
  • Justin Russell: Edmund Davy. In: Journal of Chemical Education. Band 30, Nr. 6, Juni 1953, S. 302, doi:10.1021/ed030p302.
  • Robert E. Minto, Brenda J. Blacklock: Biosynthesis and function of polyacetylenes and allied natural products. In: Progress in Lipid Research. Band 47, Nr. 4, Juli 2008, S. 233–306, doi:10.1016/j.plipres.2008.02.002, PMID 18387369, PMC 2515280 (freier Volltext).
  • Jesse A. Grantham, Richard W. McLay: Engineering Standards in Weld Failure. In: Engineering Standards for Forensic Application. Elsevier, 2019, ISBN 978-0-12-813240-1, S. 189–198, doi:10.1016/b978-0-12-813240-1.00014-5.
  • Åshild Moi Sørskår, Helge Ø. K. Stenstrøm, Yngve Stenstrøm, Simen Gjelseth Antonsen: The Alkyne Zipper Reaction: A Useful Tool in Synthetic Chemistry. In: Reactions. Band 4, Nr. 1, 30. Dezember 2022, S. 26–65, doi:10.3390/reactions4010002.
  • Peter Siemsen, Robert C. Livingston, François Diederich: Acetylenic Coupling: A Powerful Tool in Molecular Construction. In: Angewandte Chemie International Edition. Band 39, Nr. 15, 4. August 2000, S. 2632–2657, doi:10.1002/1521-3773(20000804)39:15<2632::AID-ANIE2632>3.0.CO;2-F.
  • Ullmann's Encyclopedia of Industrial Chemistry. 1. Auflage. Wiley, 2003, ISBN 3-527-30385-5, doi:10.1002/14356007.a01_097.pub4.
  • Tanaji T. Talele: Acetylene Group, Friend or Foe in Medicinal Chemistry. In: Journal of Medicinal Chemistry. Band 63, Nr. 11, 11. Juni 2020, S. 5625–5663, doi:10.1021/acs.jmedchem.9b01617.
  • Floyd L. Klavetter, Robert H. Grubbs: Polycyclooctatetraene (polyacetylene): synthesis and properties. In: Journal of the American Chemical Society. Band 110, Nr. 23, November 1988, S. 7807–7813, doi:10.1021/ja00231a036.
  • Hideki Shirakawa: The Discovery of Polyacetylene Film: The Dawning of an Era of Conducting Polymers (Nobel Lecture). In: Angewandte Chemie International Edition. Band 40, Nr. 14, 16. Juli 2001, S. 2574–2580, doi:10.1002/1521-3773(20010716)40:14<2574::AID-ANIE2574>3.0.CO;2-N.
  • C. K. Chiang, C. R. Fincher, Y. W. Park, A. J. Heeger, H. Shirakawa, E. J. Louis, S. C. Gau, Alan G. MacDiarmid: Electrical Conductivity in Doped Polyacetylene. In: Physical Review Letters. Band 39, Nr. 17, 24. Oktober 1977, S. 1098–1101, doi:10.1103/PhysRevLett.39.1098.
  • A M Sladkov, Yu P Kudryavtsev: POLYYNES. In: Russian Chemical Reviews. Band 32, Nr. 5, 31. Mai 1963, S. 229–243, doi:10.1070/RC1963v032n05ABEH001338.
  • S A Hutchinson: Biological Activities of Volatile Fungal Metabolites. In: Annual Review of Phytopathology. Band 11, Nr. 1, September 1973, S. 223–246, doi:10.1146/annurev.py.11.090173.001255.
  • Donald W. Rogers, Nikita Matsunaga, Andreas A. Zavitsas, Frank J. McLafferty, Joel F. Liebman: The Conjugation Stabilization of 1,3-Butadiyne Is Zero. In: Organic Letters. Band 5, Nr. 14, 1. Juli 2003, S. 2373–2375, doi:10.1021/ol030019h.
  • Yueze Gao, Rik R. Tykwinski: Advances in Polyynes to Model Carbyne. In: Accounts of Chemical Research. Band 55, Nr. 24, 20. Dezember 2022, S. 3616–3630, doi:10.1021/acs.accounts.2c00662.
  • Ray H. Baughman: Dangerously Seeking Linear Carbon. In: Science. Band 312, Nr. 5776, 19. Mai 2006, S. 1009–1110, doi:10.1126/science.1125999.
  • Ferdinand Bohlmann: Polyacetylene, IV. Mitteil.: Darstellung von Di‐ tert .‐butyl‐polyacetylenen. In: Chemische Berichte. Band 86, Nr. 5, Mai 1953, S. 657–667, doi:10.1002/cber.19530860519.
  • Wesley A. Chalifoux, Rik R. Tykwinski: Synthesis of polyynes to model the sp-carbon allotrope carbyne. In: Nature Chemistry. Band 2, Nr. 11, November 2010, S. 967–971, doi:10.1038/nchem.828.
  • Martin A. Bennett, Heinz P. Schwemlein: Metal Complexes of Small Cycloalkynes and Arynes. In: Angewandte Chemie International Edition in English. Band 28, Nr. 10, Oktober 1989, S. 1296–1320, doi:10.1002/anie.198912961.
  • Dieter Heber, Peter Rösner, Werner Tochtermann: Cyclooctyne and 4‐Cyclooctyn‐1‐ol – Versatile Building Blocks in Organic Synthesis. In: European Journal of Organic Chemistry. Band 2005, Nr. 20, Oktober 2005, S. 4231–4247, doi:10.1002/ejoc.200500288.
  • A. T. Blomquist, Liang Huang Liu: Many-membered Carbon Rings. VII. Cycloöctyne. In: Journal of the American Chemical Society. Band 75, Nr. 9, Mai 1953, S. 2153–2154, doi:10.1021/ja01105a039.
  • L. Brandsma, H. D. Verkruijsse: An Improved Synthesis of Cyclooctyne. In: Synthesis. Band 1978, Nr. 04, 1978, S. 290–290, doi:10.1055/s-1978-24725.
  • S. A. Krouse, R. R. Schrock, R. E. Cohen: Ring-opening polymerization of cyclooctyne. In: Macromolecules. Band 20, Nr. 4, April 1987, S. 903–904, doi:10.1021/ma00170a033.
  • Kimberly Chenoweth, David Chenoweth, William A. Goddard III: Cyclooctyne-based reagents for uncatalyzed click chemistry: A computational survey. In: Organic & Biomolecular Chemistry. Band 7, Nr. 24, 2009, S. 5255, doi:10.1039/b911482c.
  • John C. Gilbert, Everett G. McKinley, Duen-Ren Hou: The Nature of Cyclopentyne from Different Precursors. In: Tetrahedron. Band 53, Nr. 29, Juli 1997, S. 9891–9902, doi:10.1016/S0040-4020(97)00334-7.
  • Christian M. Gampe, Erick M. Carreira: Arynes and Cyclohexyne in Natural Product Synthesis. In: Angewandte Chemie International Edition. Band 51, Nr. 16, 16. April 2012, S. 3766–3778, doi:10.1002/anie.201107485.
  • Heather A. Carlson, Geoffrey E. Quelch, Henry F. Schaefer: How stable is cyclobutyne? The activation energy for the unimolecular rearrangement to butatriene. In: Journal of the American Chemical Society. Band 114, Nr. 13, Juni 1992, S. 5344–5348, doi:10.1021/ja00039a053.
  • Zhi Sun, Henry F. Schaefer: Cyclobutyne: Minimum or Transition State? In: The Journal of Organic Chemistry. Band 84, Nr. 9, 3. Mai 2019, S. 5548–5553, doi:10.1021/acs.joc.9b00502.
  • Herbert Meier, Norbert Hanold, Thomas Molz, Hans Joachim Bissinger, Heinz Kolshorn, Johannes Zountsas: Strained cycloalkenynes. In: Tetrahedron. Band 42, Nr. 6, Januar 1986, S. 1711–1719, doi:10.1016/S0040-4020(01)87588-8.
  • Dmitry V. Kuklev, Abraham J. Domb, Valery M. Dembitsky: Bioactive acetylenic metabolites. In: Phytomedicine. Band 20, Nr. 13, Oktober 2013, S. 1145–1159, doi:10.1016/j.phymed.2013.06.009.
  • Samuele Sala, Jane Fromont, Oliver Gomez, Daniel Vuong, Ernest Lacey, Gavin R. Flematti: Albanitriles A–G: Antiprotozoal Polyacetylene Nitriles from a Mycale Marine Sponge. In: Journal of Natural Products. Band 82, Nr. 12, 27. Dezember 2019, S. 3450–3455, doi:10.1021/acs.jnatprod.9b00840.
  • Edgar B. Cahoon, Judy A. Schnurr, Errol A. Huffman, Robert E. Minto: Fungal responsive fatty acid acetylenases occur widely in evolutionarily distant plant families: Fungal responsive fatty acid acetylenases. In: The Plant Journal. Band 34, Nr. 5, Juni 2003, S. 671–683, doi:10.1046/j.1365-313X.2003.01757.x.
  • K. L. Mikolajczak, C. R. Smith, M. O. Bagby, I. A. Wolff: A New Type of Naturally Occurring Polyunsaturated Fatty Acid. In: The Journal of Organic Chemistry. Band 29, Nr. 2, Februar 1964, S. 318–322, doi:10.1021/jo01025a016.
  • Kurt Aitzetmüller: Santalbic acid in the plant kingdom. In: Plant Systematics and Evolution. Band 298, Nr. 9, November 2012, S. 1609–1617, doi:10.1007/s00606-012-0678-5.
  • Marcel S. F. Lie Ken Jie, Mohammed Khysar Pasha, Fasih Ahmad: Ultrasound-assisted synthesis of santalbic acid and a study of triacylglycerol species inSantalum album (Linn.) seed oil. In: Lipids. Band 31, Nr. 10, Oktober 1996, S. 1083–1089, doi:10.1007/BF02522466.
  • D. A. Konovalov: Polyacetylene Compounds of Plants of the Asteraceae Family (Review). In: Pharmaceutical Chemistry Journal. Band 48, Nr. 9, Dezember 2014, S. 613–631, doi:10.1007/s11094-014-1159-7.
  • Leo J. Schep, Robin J. Slaughter, Gordon Becket, D. Michael G. Beasley: Poisoning due to water hemlock. In: Clinical Toxicology. Band 47, Nr. 4, April 2009, S. 270–278, doi:10.1080/15563650902904332.
  • Matthew Tcheng, Mark D. Minden, Paul A. Spagnuolo: Avocado‐derived avocadyne is a potent inhibitor of fatty acid oxidation. In: Journal of Food Biochemistry. Band 46, Nr. 3, März 2022, doi:10.1111/jfbc.13895.
  • Alex Sinclair, Robert A. Stockman: Thirty-five years of synthetic studies directed towards the histrionicotoxin family of alkaloids. In: Natural Product Reports. Band 24, Nr. 2, 2007, S. 298, doi:10.1039/b604203c.
  • John W. Blunt, Brent R. Copp, Murray H. G. Munro, Peter T. Northcote, Michèle R. Prinsep: Marine natural products. In: Natural Product Reports. Band 20, Nr. 1, 21. Januar 2003, S. 1–48, doi:10.1039/b207130b.
  • John W. Blunt, Brent R. Copp, Wan-Ping Hu, Murray H. G. Munro, Peter T. Northcote, Mich?le R. Prinsep: Marine natural products. In: Natural Product Reports. Band 24, Nr. 1, 2007, S. 31, doi:10.1039/b603047p.
  • John W. Blunt, Brent R. Copp, Wan-Ping Hu, Murray H. G. Munro, Peter T. Northcote, Michèle R. Prinsep: Marine natural products. In: Natural Product Reports. Band 26, Nr. 2, 2009, S. 170, doi:10.1039/b805113p.
  • John W. Blunt, Brent R. Copp, Murray H. G. Munro, Peter T. Northcote, Michèle R. Prinsep: Marine natural products. In: Natural Product Reports. Band 21, Nr. 1, 2004, S. 1, doi:10.1039/b305250h.
  • John W. Blunt, Brent R. Copp, Murray H. G. Munro, Peter T. Northcote, Michèle R. Prinsep: Marine natural products. In: Natural Product Reports. Band 22, Nr. 1, 2005, S. 15, doi:10.1039/b415080p.
  • Walter D. Celmer, I. A. Solomons: Mycomycin. I. Isolation, Crystallization and Chemical Characterization. In: Journal of the American Chemical Society. Band 74, Nr. 9, Mai 1952, S. 2245–2248, doi:10.1021/ja01129a024.
  • Qiu-Ye Chai, Zhen Yang, Hou-Wen Lin, Bing-Nan Han: Alkynyl-Containing Peptides of Marine Origin: A Review. In: Marine Drugs. Band 14, Nr. 11, 23. November 2016, S. 216, doi:10.3390/md14110216, PMID 27886049, PMC 5128759 (freier Volltext).
  • Mukesh C. Joshi, Diwan S. Rawat: Recent Developments in Enediyne Chemistry. In: Chemistry & Biodiversity. Band 9, Nr. 3, März 2012, S. 459–498, doi:10.1002/cbdv.201100047.
  • Matija Gredičak, Ivanka Jerić: Enediyne compounds - new promises in anticancer therapy. In: Acta Pharmaceutica. Band 57, Nr. 2, 1. Juni 2007, S. 133–150, doi:10.2478/v10007-007-0011-y.
  • Nakao Ishida, Keizō Miyazaki, Katsuo Kumagai, Mitsuo Rikimaru: Neocarzinostatin, an Antitumor Antibiotic of High Molecular Weight Isolation, Physicochemical Properties and Biological Activities. In: The Journal of Antibiotics, Series A. Band 18, Nr. 2, 1965, S. 68–76, doi:10.11554/antibioticsa.18.2_68.
  • Nada Zein, Achyut M. Sinha, William J. McGahren, George A. Ellestad: Calicheamicin γ 1 I : an Antitumor Antibiotic That Cleaves Double-Stranded DNA Site Specifically. In: Science. Band 240, Nr. 4856, 27. Mai 1988, S. 1198–1201, doi:10.1126/science.3240341.
  • Masataka Konishi, Hiroaki Ohkuma, Kyo-Ichiro Saitoh, Hiroshi Kawaguchi, Jerzy Golik, George Dubay, Gary Groenewold, Bala Krishnan, Terrence W. Doyle: Esperamicins, a novel class of potent antitumor antibiotics. I. Physico-chemical data and partial structure. In: The Journal of Antibiotics. Band 38, Nr. 11, 1985, S. 1605–1609, doi:10.7164/antibiotics.38.1605.
  • Masataka Konishi, Hiroaki Ohkuma, Kiyoshi Matsumoto, Takashi Tsuno, Hideo Kamei, Takeo Miyaki, Toshikazu Oki, Hiroshi Kawaguchi, Gregory D. Vanduyne, Jon Clardy: Dynemicin A, a novel antibiotic with the anthraquinone and 1,5-diyn-3-ene subunit. In: The Journal of Antibiotics. Band 42, Nr. 9, 1989, S. 1449–1452, doi:10.7164/antibiotics.42.1449.
  • José Cernicharo, Ana M. Heras, A. G. G. M. Tielens, Juan R. Pardo, Fabrice Herpin, Michel Guélin, L. B. F. M. Waters: [ITAL]Infrared Space Observatory's[/ITAL] Discovery of C[TINF]4[/TINF]H[TINF]2[/TINF], C[TINF]6[/TINF]H[TINF]2[/TINF], and Benzene in CRL 618. In: The Astrophysical Journal. Band 546, Nr. 2, 10. Januar 2001, S. L123–L126, doi:10.1086/318871.
  • F. Shindo, Y. Benilan, J.-C. Guillemin, P. Chaquin, A. Jolly, F. Raulin: Ultraviolet and infrared spectrum of C6H2 revisited and vapor pressure curve in Titan's atmosphere. In: Planetary and Space Science. Band 51, Nr. 1, Januar 2003, S. 9–17, doi:10.1016/S0032-0633(02)00151-4.
  • W. C. Maguire, R. A. Hanel, D. E. Jennings, V. G. Kunde, R. E. Samuelson: C3H8 and C3H4 in Titan's atmosphere. In: Nature. Band 292, Nr. 5825, August 1981, S. 683–686, doi:10.1038/292683a0.
  • Jean-Claude Guillemin, Miloud Bouyahyi, El Hassan Riague: Prebiotic, planetary and interstellar chemistry starting from compounds detected in the interstellar medium. In: Advances in Space Research. Band 33, Nr. 1, Januar 2004, S. 81–87, doi:10.1016/j.asr.2003.07.015.
  • G. P. Moss, P. A. S. Smith, D. Tavernier: Glossary of class names of organic compounds and reactivity intermediates based on structure (IUPAC Recommendations 1995). In: Pure and Applied Chemistry. Band 67, Nr. 8-9, 1. Januar 1995, S. 1307–1375, doi:10.1351/pac199567081307.
  • Angelika Fallert-Müller, Birgit Jarosch, Angela Simeon: Organische Chemie I. In: Pocket Guide Chemie. Springer Berlin Heidelberg, Berlin, Heidelberg 2019, ISBN 978-3-662-58746-1, S. 127–166, doi:10.1007/978-3-662-58747-8_4.
  • Alois Haas, Hans‐Udo Krächter: Darstellung und Reaktionen Trifluormethylchalkogenyl‐substituierter Alkine. In: Chemische Berichte. Band 121, Nr. 10, Oktober 1988, S. 1833–1840, doi:10.1002/cber.19881211023.
  • Arthur J. Hill, Floyd Tyson: STUDIES ON THE PREPARATION OF THE HIGHER ACETYLENES. I. (PRELIMINARY PAPER.) DEHALOGENATION OF 1,1-DICHLOROHEPTANE IN THE VAPOR PHASE. In: Journal of the American Chemical Society. Band 50, Nr. 1, Januar 1928, S. 172–177, doi:10.1021/ja01388a024.
  • Tsutomu Maruyama, Bunsuke Suzuki: Unsaturated Fatty Acids and Their Derivatives: Part IV. The Mechanism of Forming Stearolic Acid from Dichlorstearic Acid. In: Proceedings of the Imperial Academy. Band 7, Nr. 7, 1931, S. 265–268, doi:10.2183/pjab1912.7.265.
  • N. A. Khan, F. E. Deatherage, J. B. Brown: The preparation of stearolic acid and methyl dideutero-oleate, and certain of their derivatives. In: Journal of the American Oil Chemists Society. Band 28, Nr. 1, Januar 1951, S. 27–31, doi:10.1007/BF02639746.
  • N. A. Khan: Acetylenic compounds. I. The dehydrohalogenation reactions by sodamide in liquid ammonia and preparation of some mono-acetylenic substances and their derivatives. In: Journal of the American Oil Chemists Society. Band 30, Nr. 9, September 1953, S. 355–358, doi:10.1007/BF02633768.
  • John R. Johnson, W. L. McEwen: THE IDENTIFICATION OF MONOSUBSTITUTED ACETYLENES. DERIVATIVES OF DIETHINYL MERCURY. In: Journal of the American Chemical Society. Band 48, Nr. 2, Februar 1926, S. 469–476, doi:10.1021/ja01413a025.
  • Damien Habrant, Vesa Rauhala, Ari M. P. Koskinen: Conversion of carbonyl compounds to alkynes: general overview and recent developments. In: Chemical Society Reviews. Band 39, Nr. 6, 2010, S. 2007, doi:10.1039/b915418c.
  • E.J. Corey, P.L. Fuchs: A synthetic method for formyl→ethynyl conversion (RCHO→RC≡CH or RC≡CR′). In: Tetrahedron Letters. Band 13, Nr. 36, 1972, S. 3769–3772, doi:10.1016/S0040-4039(01)94157-7.
  • Frédéric Eymery, Bogdan Iorga, Philippe Savignac: The Usefulness of Phosphorus Compounds in Alkyne Synthesis. In: Synthesis. Band 2000, Nr. 02, 2000, S. 185–213, doi:10.1055/s-2000-6241.
  • Patrick Michel, Dominique Gennet, André Rassat: A one-pot procedure for the synthesis of alkynes and bromoalkynes from aldehydes. In: Tetrahedron Letters. Band 40, Nr. 49, Dezember 1999, S. 8575–8578, doi:10.1016/S0040-4039(99)01830-4.
  • Ernest W. Colvin, Brendan J. Hamill: One-step conversion of carbonyl compounds into acetylenes. In: Journal of the Chemical Society, Chemical Communications. Nr. 5, 1973, S. 151, doi:10.1039/c39730000151.
  • Kazuhiro Miwa, Toyohiko Aoyama, Takayuki Shioiri: Extension of the Colvin Rearrangement Using Trimethylsilyldiazomethane. A New Synthesis of Alkynes. In: Synlett. Band 1994, Nr. 02, 1994, S. 107–108, doi:10.1055/s-1994-22755.
  • Douglass F. Taber, Sha Bai, Peng-fei Guo: A convenient reagent for aldehyde to alkyne homologation. In: Tetrahedron Letters. Band 49, Nr. 48, November 2008, S. 6904–6906, doi:10.1016/j.tetlet.2008.09.114, PMID 19946355, PMC 2634292 (freier Volltext).
  • Y. Taguchi, H. Endo, Y. Abe, J. Matsumoto, T. Wakabayashi, T. Kodama, Y. Achiba, H. Shiromaru: Polyyne formation by graphite laser ablation in argon and propane mixed gases. In: Carbon. Band 94, November 2015, S. 124–128, doi:10.1016/j.carbon.2015.06.058.
  • Seung Keun Shin, Jae Kyu Song, Seung Min Park: Preparation of polyynes by laser ablation of graphite in aqueous media. In: Applied Surface Science. Band 257, Nr. 12, April 2011, S. 5156–5158, doi:10.1016/j.apsusc.2010.10.074.
  • Masaharu Tsuji, Takeshi Tsuji, Shingo Kuboyama, Seong-Ho Yoon, Yozo Korai, Teppei Tsujimoto, Kanji Kubo, Akira Mori, Isao Mochida: Formation of hydrogen-capped polyynes by laser ablation of graphite particles suspended in solution. In: Chemical Physics Letters. Band 355, Nr. 1-2, März 2002, S. 101–108, doi:10.1016/S0009-2614(02)00192-6.
  • Franco Cataldo: Polyynes and cyanopolyynes synthesis from the submerged electric arc: about the role played by the electrodes and solvents in polyynes formation. In: Tetrahedron. Band 60, Nr. 19, Mai 2004, S. 4265–4274, doi:10.1016/j.tet.2004.03.033.
  • Alois Fürstner, Paul W. Davies: Alkyne metathesis. In: Chemical Communications. Nr. 18, 2005, S. 2307, doi:10.1039/b419143a.
  • Tadashi Eguchi, Kenji Arakawa, Katsumi Kakinuma: Synthesis of over 30-Membered Giant Ring Compounds. Synthetic Study of Archaeal 36- and 72-Membered Macrocyclic Membrane Lipids. In: Journal of Synthetic Organic Chemistry, Japan. Band 57, Nr. 9, 1999, S. 784–797, doi:10.5059/yukigoseikyokaishi.57.784.
  • Rolf Gleiter: Cycloalkadiynes—From Bent Triple Bonds to Strained Cage Compounds. In: Angewandte Chemie International Edition in English. Band 31, Nr. 1, Januar 1992, S. 27–44, doi:10.1002/anie.199200271.
  • Robert A. Benkeser, Gene Schroll, Dale M. Sauve: Reduction of Organic Compounds by Lithium in Low Molecular Weight Amines. II. Stereochemistry. Chemical Reduction of an Isolated Non-terminal Double Bond. In: Journal of the American Chemical Society. Band 77, Nr. 12, Juni 1955, S. 3378–3379, doi:10.1021/ja01617a066.
  • Herbert O. House, Edith F. Kinloch: Reactions involving electron transfer. V. Reduction on nonconjugated acetylenes. In: The Journal of Organic Chemistry. Band 39, Nr. 6, März 1974, S. 747–755, doi:10.1021/jo00920a002.
  • Paul J. Kropp, Scott D. Crawford: Surface-Mediated Reactions. 4. Hydrohalogenation of Alkynes. In: The Journal of Organic Chemistry. Band 59, Nr. 11, Juni 1994, S. 3102–3112, doi:10.1021/jo00090a031.
  • Robert C. Fahey, Do-Jae Lee: Polar additions to olefins and acetylenes. V. Bimolecular and termolecular mechanisms in the hydrochlorination of acetylenes. In: Journal of the American Chemical Society. Band 90, Nr. 8, April 1968, S. 2124–2131, doi:10.1021/ja01010a034.
  • Suzanne R. Macaulay: The rearrangement of isomeric linear decyn-1-ols by reaction with the sodium salt of 1,3-diaminopropane. In: Canadian Journal of Chemistry. Band 58, Nr. 23, 1. Dezember 1980, S. 2567–2572, doi:10.1139/v80-409.
  • Charles Allan Brown, Ayako Yamashita: Saline hydrides and superbases in organic reactions. IX. Acetylene zipper. Exceptionally facile contrathermodynamic multipositional isomerization of alkynes with potassium 3-aminopropylamide. In: Journal of the American Chemical Society. Band 97, Nr. 4, Februar 1975, S. 891–892, doi:10.1021/ja00837a034.
  • Kiitiro Utimoto, Michio Tanaka, Mitsumasa Kitai, Hitosi Nozaki: Cyclization of ω-trimethylsilylethynylalkanoyl chlorides. Application of the preparation of large ring ynones and dl- and (R)-muscone. In: Tetrahedron Letters. Band 19, Nr. 26, 1. Januar 1978, S. 2301–2304, doi:10.1016/S0040-4039(01)91520-5.
  • Kenji Mori, Narshinha P. Argade: Pheromone Synthesis, CLXIII. Synthesis of (9Z,25S,26R,43Z)-25,26-Epoxy-9,43-henpentacontadiene and Its Antipode, Components of the Nymph Recognition Pheromone Produced by Nymphs of the CockroachNauphoeta cinerea. In: Liebigs Annalen der Chemie. Band 1994, Nr. 7, 12. Juli 1994, S. 695–700, doi:10.1002/jlac.199419940711.
  • Vitor L. S. Cunha, Xiaofan Liu, Todd L. Lowary, George A. O’Doherty: De Novo Asymmetric Synthesis of Avocadyne, Avocadene, and Avocadane Stereoisomers. In: The Journal of Organic Chemistry. Band 84, Nr. 23, 24. Oktober 2019, S. 15718–15725, doi:10.1021/acs.joc.9b02391.
  • Nabil Tahiri, Peter Fodran, Dhineshkumar Jayaraman, Jeffrey Buter, Martin D. Witte, Tonatiuh A. Ocampo, D. Branch Moody, Ildiko Van Rhijn, Adriaan J. Minnaard: Total Synthesis of a Mycolic Acid from Mycobacterium tuberculosis. In: Angewandte Chemie International Edition. Band 59, Nr. 19, 10. März 2020, S. 7555–7560, doi:10.1002/anie.202000523, PMID 32067294, PMC 7216993 (freier Volltext).
  • Jack E. Baldwin: Rules for ring closure. In: Journal of the Chemical Society, Chemical Communications. Nr. 18, 1976, S. 734, doi:10.1039/c39760000734.
  • Kerry Gilmore, Rana K. Mohamed, Igor V. Alabugin: The Baldwin rules: revised and extended: Baldwin: Revised, Extended. In: Wiley Interdisciplinary Reviews: Computational Molecular Science. Band 6, Nr. 5, September 2016, S. 487–514, doi:10.1002/wcms.1261.
  • Igor V. Alabugin, Kerry Gilmore: Finding the right path: Baldwin “Rules for Ring Closure” and stereoelectronic control of cyclizations. In: Chemical Communications. Band 49, Nr. 96, 2013, S. 11246, doi:10.1039/c3cc43872d.
  • Kerry Gilmore, Igor V. Alabugin: Cyclizations of Alkynes: Revisiting Baldwin’s Rules for Ring Closure. In: Chemical Reviews. Band 111, Nr. 11, 9. November 2011, S. 6513–6556, doi:10.1021/cr200164y.
  • Noriyuki Takanashi, Kenta Suzuki, Mariko Kitajima, Hiromitsu Takayama: Total synthesis of conolidine and apparicine. In: Tetrahedron Letters. Band 57, Nr. 3, Januar 2016, S. 375–378, doi:10.1016/j.tetlet.2015.12.029.
  • Karl Kirchner, Maria José Calhorda, Roland Schmid, Luís F. Veiros: Mechanism for the Cyclotrimerization of Alkynes and Related Reactions Catalyzed by CpRuCl. In: Journal of the American Chemical Society. Band 125, Nr. 38, 1. September 2003, S. 11721–11729, doi:10.1021/ja035137e.
  • Yoshihiko Yamamoto: Recent Advances in Intramolecular Alkyne Cyclotrimerization and Its Applications. In: Current Organic Chemistry. Band 9, Nr. 6, S. 503–519, doi:10.2174/1385272053544399.
  • Pablo Wessig, Gunnar Müller: The Dehydro-Diels−Alder Reaction. In: Chemical Reviews. Band 108, Nr. 6, 1. Juni 2008, S. 2051–2063, doi:10.1021/cr0783986.
  • Wenbo Li, Liejin Zhou, Junliang Zhang: Recent Progress in Dehydro(genative) Diels–Alder Reaction. In: Chemistry – A European Journal. Band 22, Nr. 5, 26. Januar 2016, S. 1558–1571, doi:10.1002/chem.201503571.
  • Alexander Z. Bradley, Richard P. Johnson: Thermolysis of 1,3,8-Nonatriyne: Evidence for Intramolecular [2 + 4] Cycloaromatization to a Benzyne Intermediate. In: Journal of the American Chemical Society. Band 119, Nr. 41, 1. Oktober 1997, S. 9917–9918, doi:10.1021/ja972141f.
  • Ok Ton Dyan, Gennady I. Borodkin, Pavel A. Zaikin: The Diels–Alder Reaction for the Synthesis of Polycyclic Aromatic Compounds. In: European Journal of Organic Chemistry. Band 2019, Nr. 44, 30. November 2019, S. 7271–7306, doi:10.1002/ejoc.201901254.
  • Young Keun Chung: Transition metal alkyne complexes: the Pauson–Khand reaction. In: Coordination Chemistry Reviews. Band 188, Nr. 1, Juli 1999, S. 297–341, doi:10.1016/S0010-8545(99)00032-6.
  • Rodney A. Fernandes, Anupama Kumari, Ramdas S. Pathare: A Decade with Dötz Benzannulation in the Synthesis of Natural Products. In: Synlett. Band 31, Nr. 05, März 2020, S. 403–420, doi:10.1055/s-0039-1690791.
  • Janet Wisniewski Grissom, Gamini U. Gunawardena, Detlef Klingberg, Dahai Huang: The chemistry of enediynes, enyne allenes and related compounds. In: Tetrahedron. Band 52, Nr. 19, Mai 1996, S. 6453–6518, doi:10.1016/0040-4020(96)00016-6.
  • Matija Gredičak, Ivanka Jerić: Enediyne compounds - new promises in anticancer therapy. In: Acta Pharmaceutica. Band 57, Nr. 2, 1. Juni 2007, S. 133–150, doi:10.2478/v10007-007-0011-y.
  • Richard R. Jones, Robert G. Bergman: p-Benzyne. Generation as an intermediate in a thermal isomerization reaction and trapping evidence for the 1,4-benzenediyl structure. In: Journal of the American Chemical Society. Band 94, Nr. 2, Januar 1972, S. 660–661, doi:10.1021/ja00757a071.
  • Patrick W. Musch, Christian Remenyi, Holger Helten, Bernd Engels: On the Regioselectivity of the Cyclization of Enyne−Ketenes: A Computational Investigation and Comparison with the Myers-Saito and Schmittel Reaction. In: Journal of the American Chemical Society. Band 124, Nr. 8, 1. Februar 2002, S. 1823–1828, doi:10.1021/ja017532f.
  • Michael Schmittel, Marc Strittmatter, Susanne Kiau: Switching from the Myers reaction to a new thermal cyclization mode in enyne-allenes. In: Tetrahedron Letters. Band 36, Nr. 28, Juli 1995, S. 4975–4978, doi:10.1016/0040-4039(95)00937-8.
  • Shivalinga Kolle, Sanjay Batra: Transformations of alkynes to carboxylic acids and their derivatives via CC bond cleavage. In: Organic & Biomolecular Chemistry. Band 14, Nr. 47, 2016, S. 11048–11060, doi:10.1039/C6OB01912A.
  • Tanveer Mahamadali Shaikh, Fung-E Hong: Iron-Catalyzed Oxidative Cleavage of Olefins and Alkynes to Carboxylic Acids with Aqueous tert-Butyl Hydroperoxide. In: Advanced Synthesis & Catalysis. Band 353, Nr. 9, Juni 2011, S. 1491–1496, doi:10.1002/adsc.201000899.
  • F. Pennella, R. L. Banks, G. C. Bailey: Disproportionation of alkynes. In: Chemical Communications (London). Nr. 23, 1968, S. 1548, doi:10.1039/c19680001548.
  • André Mortreux, Michel Blanchard: Metathesis of alkynes by a molybdenum hexacarbonyl–resorcinol catalyst. In: J. Chem. Soc., Chem. Commun. Nr. 19, 1974, S. 786–787, doi:10.1039/C39740000786.
  • Alois Fürstner, Günter Seidel: Ring closing alkyne metathesis: stereoselective synthesis of civetone. In: Journal of Organometallic Chemistry. Band 606, Nr. 1, Juli 2000, S. 75–78, doi:10.1016/S0022-328X(00)00096-6.
  • Alois Fürstner, Oliver Guth, Antonio Rumbo, Günter Seidel: Ring Closing Alkyne Metathesis. Comparative Investigation of Two Different Catalyst Systems and Application to the Stereoselective Synthesis of Olfactory Lactones, Azamacrolides, and the Macrocyclic Perimeter of the Marine Alkaloid Nakadomarin A. In: Journal of the American Chemical Society. Band 121, Nr. 48, 1. Dezember 1999, S. 11108–11113, doi:10.1021/ja992074k.
  • Miwako Mori: Synthesis of Natural Products and Related Compounds using Enyne Metathesis. In: Advanced Synthesis & Catalysis. Band 349, Nr. 1-2, 8. Januar 2007, S. 121–135, doi:10.1002/adsc.200600484.
  • Miwako Mori, Tomohiro Tomita, Yoichi Kita, Tsuyoshi Kitamura: Synthesis of (+)-anatoxin-a using enyne metathesis. In: Tetrahedron Letters. Band 45, Nr. 22, Mai 2004, S. 4397–4399, doi:10.1016/j.tetlet.2004.03.171.
  • Jehrod B. Brenneman, Rainer Machauer, Stephen F. Martin: Enantioselective synthesis of (+)-anatoxin-a via enyne metathesis. In: Tetrahedron. Band 60, Nr. 34, August 2004, S. 7301–7314, doi:10.1016/j.tet.2004.06.021.
  • Yajing Liu, Jacky W. Y. Lam, Ben Zhong Tang: Conjugated polymers developed from alkynes. In: National Science Review. Band 2, Nr. 4, 1. Dezember 2015, S. 493–509, doi:10.1093/nsr/nwv047.
  • Rongrong Hu, Weizhang Li, Ben Zhong Tang: Recent Advances in Alkyne-Based Multicomponent Polymerizations. In: Macromolecular Chemistry and Physics. Band 217, Nr. 2, Januar 2016, S. 213–224, doi:10.1002/macp.201500291.
  • Rongrong Hu, Jacky W. Y. Lam, Min Li, Haiqin Deng, Jie Li, Ben Zhong Tang: Homopolycyclotrimerization of A 4 -type tetrayne: A new approach for the creation of a soluble hyperbranched poly(tetraphenylethene) with multifunctionalities. In: Journal of Polymer Science Part A: Polymer Chemistry. Band 51, Nr. 22, 15. November 2013, S. 4752–4764, doi:10.1002/pola.26897.
  • Anjun Qin, Jacky W. Y. Lam, Ben Zhong Tang: Click polymerization. In: Chemical Society Reviews. Band 39, Nr. 7, 2010, S. 2522, doi:10.1039/b909064a.
  • Hong-kun Li, Jing-zhi Sun, An-jun Qin, Ben Zhong Tang: Azide-alkyne click polymerization: An update. In: Chinese Journal of Polymer Science. Band 30, Nr. 1, Januar 2012, S. 1–15, doi:10.1007/s10118-012-1098-2.
  • James R. Green: Chemistry of Propargyldicobalt Cations Recent Developments in the Nicholas and Related Reactions. In: Current Organic Chemistry. Band 5, Nr. 7, S. 809–826, doi:10.2174/1385272013375247.
  • John R. Grunwell, Michael F. Wempe, Judith Mitchell, Jocelyn R. Grunwell: The transannular rearrangement of 5-cyclodecynone. In: Tetrahedron Letters. Band 34, Nr. 45, November 1993, S. 7163–7166, doi:10.1016/S0040-4039(00)79277-X.
  • Rafael Chinchilla, Carmen Nájera: Recent advances in Sonogashira reactions. In: Chemical Society Reviews. Band 40, Nr. 10, 2011, S. 5084, doi:10.1039/c1cs15071e.
  • Rafael Chinchilla, Carmen Nájera: The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry. In: Chemical Reviews. Band 107, Nr. 3, 1. März 2007, S. 874–922, doi:10.1021/cr050992x.
  • Dan Wang, Shuanhu Gao: Sonogashira coupling in natural product synthesis. In: Org. Chem. Front. Band 1, Nr. 5, 2014, S. 556–566, doi:10.1039/C3QO00086A.
  • Toyonobu Usuki, Haruka Yamada, Takahiro Hayashi, Hiroto Yanuma, Yohei Koseki, Noriyuki Suzuki, Yoshiro Masuyama, Yong Y. Lin: Total synthesis of COPD biomarker desmosine that crosslinks elastin. In: Chemical Communications. Band 48, Nr. 26, 2012, S. 3233, doi:10.1039/c2cc17958j.
  • Belén Vaz, Leticia Otero, Rosana Álvarez, Ángel R. de Lera: Total Synthesis of Enantiopure Pyrrhoxanthin: Alternative Methods for the Stereoselective Preparation of 4-Alkylidenebutenolides. In: Chemistry - A European Journal. Band 19, Nr. 39, 23. September 2013, S. 13065–13074, doi:10.1002/chem.201301873.
  • Glaser coupling. In: Name Reactions. Springer Berlin Heidelberg, Berlin, Heidelberg 2006, ISBN 3-540-30030-9, S. 263–264, doi:10.1007/3-540-30031-7_117.
  • Siqi Zhang, Liang Zhao: A merged copper(I/II) cluster isolated from Glaser coupling. In: Nature Communications. Band 10, Nr. 1, 24. Oktober 2019, doi:10.1038/s41467-019-12889-w, PMID 31649254, PMC 6813345 (freier Volltext).
  • Allan S. Hay: Oxidative Coupling of Acetylenes. II 1. In: The Journal of Organic Chemistry. Band 27, Nr. 9, September 1962, S. 3320–3321, doi:10.1021/jo01056a511.
  • Wei Shi, Aiwen Lei: 1,3-Diyne chemistry: synthesis and derivations. In: Tetrahedron Letters. Band 55, Nr. 17, April 2014, S. 2763–2772, doi:10.1016/j.tetlet.2014.03.022.
  • Guoli Mo, Zaimin Tian, Jiping Li, Guohua Wen, Xiaomin Yang: Silver-catalyzed Glaser coupling of alkynes: Silver-catalyzed Glaser coupling of alkynes. In: Applied Organometallic Chemistry. Band 29, Nr. 4, April 2015, S. 231–233, doi:10.1002/aoc.3275.
  • Riccardo F. Carina, Christiane Dietrich-Buchecker, Jean-Pierre Sauvage: Molecular Composite Knots. In: Journal of the American Chemical Society. Band 118, Nr. 38, 1. Januar 1996, S. 9110–9116, doi:10.1021/ja961459p.
  • Carin C. C. Johansson Seechurn, Matthew O. Kitching, Thomas J. Colacot, Victor Snieckus: Palladium-Catalyzed Cross-Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize. In: Angewandte Chemie International Edition. Band 51, Nr. 21, 21. Mai 2012, S. 5062–5085, doi:10.1002/anie.201107017.
  • John E. Moses, Adam D. Moorhouse: The growing applications of click chemistry. In: Chem. Soc. Rev. Band 36, Nr. 8, 2007, S. 1249–1262, doi:10.1039/B613014N.
  • Wolfgang H. Binder, Christian Kluger: Azide/Alkyne-“Click” Reactions: Applications in Material Science and Organic Synthesis. In: Current Organic Chemistry. Band 10, Nr. 14, S. 1791–1815, doi:10.2174/138527206778249838.
  • Jean-François Lutz, Zoya Zarafshani: Efficient construction of therapeutics, bioconjugates, biomaterials and bioactive surfaces using azide–alkyne “click” chemistry. In: Advanced Drug Delivery Reviews. Band 60, Nr. 9, Juni 2008, S. 958–970, doi:10.1016/j.addr.2008.02.004.
  • Chao-Jun Li: The Development of Catalytic Nucleophilic Additions of Terminal Alkynes in Water. In: Accounts of Chemical Research. Band 43, Nr. 4, 20. April 2010, S. 581–590, doi:10.1021/ar9002587.
  • E. Yu. Shmidt, I. A. Bidusenko, N. I. Protsuk, A. I. Mikhaleva, B. A. Trofimov: Improved synthesis of tertiary propargyl alcohols by the Favorskii reaction of alkyl aryl (hetaryl) ketones with acetylene. In: Russian Journal of Organic Chemistry. Band 49, Nr. 1, Januar 2013, S. 8–11, doi:10.1134/S1070428013010028.
  • Tao Shen, Teng Wang, Chong Qin, Ning Jiao: Silver-Catalyzed Nitrogenation of Alkynes: A Direct Approach to Nitriles through C≡C Bond Cleavage. In: Angewandte Chemie International Edition. Band 52, Nr. 26, 24. Juni 2013, S. 6677–6680, doi:10.1002/anie.201300193.
  • Alexander Ernst, Luca Gobbi, Andrea Vasella: Orthogonally protected dialkynes. In: Tetrahedron Letters. Band 37, Nr. 44, Oktober 1996, S. 7959–7962, doi:10.1016/0040-4039(96)01838-2.
  • Xin Yang, Daisuke Matsuo, Yoshinori Suzuma, Jing-Kun Fang, Feng Xu, Akihiro Orita, Junzo Otera, Shingo Kajiyama, Nagatoshi Koumura, Kohjiro Hara: Ph2P(O) Group for Protection of Terminal Acetylenes. In: Synlett. Band 2011, Nr. 16, Oktober 2011, S. 2402–2406, doi:10.1055/s-0030-1261223.
  • Reinhard Nast: Coordination chemistry of metal alkynyl compounds. In: Coordination Chemistry Reviews. Band 47, Nr. 1-2, November 1982, S. 89–124, doi:10.1016/0010-8545(82)85011-X.
  • Umberto Belluco, Roberta Bertani, Rino A. Michelin, Mirto Mozzon: Platinum—alkynyl and —alkyne complexes: old systems with new chemical and physical perspectives. In: Journal of Organometallic Chemistry. Band 600, Nr. 1-2, April 2000, S. 37–55, doi:10.1016/S0022-328X(00)00089-9.
  • Helmut Werner: Organometallic chemistry of alkenes and alkynes. In: Journal of Organometallic Chemistry. Band 475, Nr. 1-2, Juli 1994, S. 45–55, doi:10.1016/0022-328X(94)84006-7.
  • Zheng Lu, Khalil A. Abboud, W. M. Jones: Platinum(0) complexes of cyclic alkynes and allenes from base-induced dehydrohalogenation of bromocycloalkenes. In: Organometallics. Band 12, Nr. 4, April 1993, S. 1471–1474, doi:10.1021/om00028a079.
  • Martin A. Bennett, Heinz P. Schwemlein: Metall-Komplexe mit kleinen Cycloalkinen und Arinen. In: Angewandte Chemie. Band 101, Nr. 10, Oktober 1989, S. 1349–1373, doi:10.1002/ange.19891011006.
  • Ioan-Teodor Trotuş, Tobias Zimmermann, Ferdi Schüth: Catalytic Reactions of Acetylene: A Feedstock for the Chemical Industry Revisited. In: Chemical Reviews. Band 114, Nr. 3, 12. Februar 2014, S. 1761–1782, doi:10.1021/cr400357r.
  • Ahmed E. S. Nosseir, Angelo Cervone, Angelo Pasini: Review of State-of-the-Art Green Monopropellants: For Propulsion Systems Analysts and Designers. In: Aerospace. Band 8, Nr. 1, 15. Januar 2021, S. 20, doi:10.3390/aerospace8010020.
  • S.D.T. Maduwanthi, R.A.U.J. Marapana: Comparison of pigments and some physicochemical properties of banana as affected by ethephon and acetylene induced ripening. In: Biocatalysis and Agricultural Biotechnology. Band 33, Mai 2021, S. 101997, doi:10.1016/j.bcab.2021.101997.
  • S. D. T. Maduwanthi, R. A. U. J. Marapana: Induced Ripening Agents and Their Effect on Fruit Quality of Banana. In: International Journal of Food Science. Band 2019, 2. Mai 2019, S. 1–8, doi:10.1155/2019/2520179, PMID 31187037, PMC 6521425 (freier Volltext).
  • Frank Z. Stanczyk, David F. Archer, Bhagu R. Bhavnani: Ethinyl estradiol and 17β-estradiol in combined oral contraceptives: pharmacokinetics, pharmacodynamics and risk assessment. In: Contraception. Band 87, Nr. 6, Juni 2013, S. 706–727, doi:10.1016/j.contraception.2012.12.011.
  • Dennis R. Doose, Shean-Sheng Wang, Mukund Padmanabhan, Stefan Schwabe, David Jacobs, Meir Bialer: Effect of Topiramate or Carbamazepine on the Pharmacokinetics of an Oral Contraceptive Containing Norethindrone and Ethinyl Estradiol in Healthy Obese and Nonobese Female Subjects. In: Epilepsia. Band 44, Nr. 4, 10. April 2003, S. 540–549, doi:10.1046/j.1528-1157.2003.55602.x.
  • Frank Z. Stanczyk, David F. Archer: Gestodene: A review of its pharmacology, potency and tolerability in combined contraceptive preparations. In: Contraception. Band 89, Nr. 4, April 2014, S. 242–252, doi:10.1016/j.contraception.2013.12.003.
  • Antony Stewart, Carole Cummins, Lisa Gold, Rachel Jordan, Wendy Phillips: The effectiveness of the levonorgestrel-releasing intrauterine system in menorrhagia: a systematic review. In: British Journal of Obstetrics and Gynaecology. Band 108, Nr. 1, Januar 2001, S. 74–86, doi:10.1016/S0306-5456(00)00020-6.
  • Kusum V. Moray, Himanshu Chaurasia, Oshima Sachin, Beena Joshi: A systematic review on clinical effectiveness, side-effect profile and meta-analysis on continuation rate of etonogestrel contraceptive implant. In: Reproductive Health. Band 18, Nr. 1, Dezember 2021, doi:10.1186/s12978-020-01054-y, PMID 33407632, PMC 7788930 (freier Volltext).
  • M Babják, G Balogh, M Gazdag, S Görög: Estimation of impurity profiles of drugs and related materials. In: Journal of Pharmaceutical and Biomedical Analysis. Band 29, Nr. 6, August 2002, S. 1153–1157, doi:10.1016/S0731-7085(02)00165-6.
  • Susan S. Jick, James A. Kaye, Stefan Russmann, Hershel Jick: Risk of nonfatal venous thromboembolism in women using a contraceptive transdermal patch and oral contraceptives containing norgestimate and 35 μg of ethinyl estradiol. In: Contraception. Band 73, Nr. 3, März 2006, S. 223–228, doi:10.1016/j.contraception.2006.01.001.
  • Karen L Goa, Gregory T Warner, Stephanie E Easthope: Transdermal Ethinylestradiol/Norelgestromin: A Review of its Use in Hormonal Contraception. In: Treatments in Endocrinology. Band 2, Nr. 3, 2003, S. 191–206, doi:10.2165/00024677-200302030-00005.
  • Eric A. Schaff: Mifepristone: ten years later. In: Contraception. Band 81, Nr. 1, Januar 2010, S. 1–7, doi:10.1016/j.contraception.2009.08.004.
  • Herbert Kuhl: Pharmacology of estrogens and progestogens: influence of different routes of administration. In: Climacteric. 2005, Band 8, Nummer sup1, S. 3–63. doi:10.1080/13697130500148875.
  • Richard Godin, Violaine Marcoux: Vaginally Administered Danazol: An Overlooked Option in the Treatment of Rectovaginal Endometriosis? In: Journal of Obstetrics and Gynaecology Canada. Band 37, Nr. 12, Dezember 2015, S. 1098–1103, doi:10.1016/S1701-2163(16)30075-5.
  • Tamás Tábi, László Vécsei, Moussa B. Youdim, Peter Riederer, Éva Szökő: Selegiline: a molecule with innovative potential. In: Journal of Neural Transmission. Band 127, Nr. 5, Mai 2020, S. 831–842, doi:10.1007/s00702-019-02082-0, PMID 31562557, PMC 7242272 (freier Volltext).
  • Vicki Oldfield, Gillian M Keating, Caroline M Perry: Rasagiline: A Review of its Use in the Management of Parkinson??s Disease. In: Drugs. Band 67, Nr. 12, 2007, S. 1725–1747, doi:10.2165/00003495-200767120-00006.
  • Rok Borštnar, Matej Repič, Mojca Kržan, Janez Mavri, Robert Vianello: Irreversible Inhibition of Monoamine Oxidase B by the Antiparkinsonian Medicines Rasagiline and Selegiline: A Computational Study. In: European Journal of Organic Chemistry. 2011, Band 2011, Nummer 32, S. 6419–6433 doi:10.1002/ejoc.201100873.
  • G. M. Everett, L. E. Blockus, I. M. Shepperd: Tremor Induced by Tremorine and Its Antagonism by Anti-Parkinson Drugs. In: Science. Band 124, Nr. 3211, 1956, S. 79–79, doi:10.1126/science.124.3211.79.a.
  • Jin H. Park, Yingting Liu, Mark A. Lemmon, Ravi Radhakrishnan: Erlotinib binds both inactive and active conformations of the EGFR tyrosine kinase domain. In: Biochemical Journal. Band 448, Nr. 3, 15. Dezember 2012, S. 417–423, doi:10.1042/BJ20121513, PMID 23101586, PMC 3507260 (freier Volltext).
  • Jonathan Dowell, John D. Minna, Peter Kirkpatrick: Erlotinib hydrochloride. In: Nature Reviews Drug Discovery. Band 4, Nr. 1, Januar 2005, S. 13–14, doi:10.1038/nrd1612.
  • N. Spellmon, C. Li, Z. Yang: Allosterically targeting EGFR drug-resistance gatekeeper mutations. In: Journal of thoracic disease. Band 9, Nummer 7, Juli 2017, S. 1756–1758, doi:10.21037/jtd.2017.06.43, PMID 28839955, PMC 5542946 (freier Volltext).
  • Xiaohai Li, Theodore M. Kamenecka, Michael D. Cameron: Cytochrome P450-Mediated Bioactivation of the Epidermal Growth Factor Receptor Inhibitor Erlotinib to a Reactive Electrophile. In: Drug Metabolism and Disposition. Band 38, Nr. 7, Juli 2010, S. 1238–1245, doi:10.1124/dmd.109.030361, PMID 20382753, PMC 3202369 (freier Volltext).
  • Yahiya Y. Syed: Futibatinib: First Approval. In: Drugs. Band 82, Nr. 18, Dezember 2022, S. 1737–1743, doi:10.1007/s40265-022-01806-z.
  • Juliana T. W. Tong, Paul W. R. Harris, Margaret A. Brimble, Iman Kavianinia: An Insight into FDA Approved Antibody-Drug Conjugates for Cancer Therapy. In: Molecules. Band 26, Nr. 19, 27. September 2021, S. 5847, doi:10.3390/molecules26195847, PMID 34641391, PMC 8510272 (freier Volltext).
  • Yvette N. Lamb: Inotuzumab Ozogamicin: First Global Approval. In: Drugs. Band 77, Nr. 14, September 2017, S. 1603–1610, doi:10.1007/s40265-017-0802-5.
  • Alejandro D. Ricart: Antibody-Drug Conjugates of Calicheamicin Derivative: Gemtuzumab Ozogamicin and Inotuzumab Ozogamicin. In: Clinical Cancer Research. Band 17, Nr. 20, 15. Oktober 2011, S. 6417–6427, doi:10.1158/1078-0432.CCR-11-0486.
  • Gary S. Wood, Jianqiang Wu: Methotrexate and Pralatrexate. In: Dermatologic Clinics. Band 33, Nr. 4, Oktober 2015, S. 747–755, doi:10.1016/j.det.2015.05.009, PMID 26433846, PMC 5549926 (freier Volltext).
  • Lyn C. Guenther: Optimizing Treatment with Topical Tazarotene:. In: American Journal of Clinical Dermatology. Band 4, Nr. 3, 2003, S. 197–202, doi:10.2165/00128071-200304030-00006.
  • Saskia ME Vrouenraets, Ferdinand WNM Wit, Jacqueline van Tongeren, Joep MA Lange: Efavirenz: a review. In: Expert Opinion on Pharmacotherapy. Band 8, Nr. 6, April 2007, S. 851–871, doi:10.1517/14656566.8.6.851.
  • Julia Paik: Lenacapavir: First Approval. In: Drugs. Band 82, Nr. 14, September 2022, S. 1499–1504, doi:10.1007/s40265-022-01786-0, PMID 36272024, PMC 10267266 (freier Volltext).
  • Michele Baldrighi, Davide Bartesaghi, Gabriella Cavallo, Michele R. Chierotti, Roberto Gobetto, Pierangelo Metrangolo, Tullio Pilati, Giuseppe Resnati, Giancarlo Terraneo: Polymorphs and co-crystals of haloprogin: an antifungal agent. In: CrystEngComm. Band 16, Nr. 26, 2014, S. 5897–5904, doi:10.1039/C4CE00367E.
  • S Krishnan-Natesan: Terbinafine: a pharmacological and clinical review. In: Expert Opinion on Pharmacotherapy. Band 10, Nr. 16, November 2009, S. 2723–2733, doi:10.1517/14656560903307462.
  • Kelly Jirschele, Peter K. Sand: Oxybutynin: past, present, and future. In: International Urogynecology Journal. Band 24, Nr. 4, April 2013, S. 595–604, doi:10.1007/s00192-012-1915-8.
  • H. Olschewski: Inhaled iloprost for the treatment of pulmonary hypertension. In: European Respiratory Review. Band 18, Nr. 111, 1. März 2009, S. 29–34, doi:10.1183/09059180.00011111.
  • Marzieh Hashemi, Avat (Arman) Taherpour: Theoretical kinetic and thermodynamic studies of the strain energies and ring size effects of the 1,3-dipolar cycloaddition reactions on ethinamate medicine analogs. In: Journal of Molecular Structure. Band 1204, März 2020, S. 127544, doi:10.1016/j.molstruc.2019.127544.
  • Ulrike Graefe-Mody, Silke Retlich, Christian Friedrich: Clinical Pharmacokinetics and Pharmacodynamics of Linagliptin:. In: Clinical Pharmacokinetics. Band 51, Nr. 7, Juli 2012, S. 411–427, doi:10.2165/11630900-000000000-00000.
  • Clemens Lamberth: Alkyne chemistry in crop protection. In: Bioorganic & Medicinal Chemistry. Band 17, Nr. 12, Juni 2009, S. 4047–4063, doi:10.1016/j.bmc.2008.11.037.
  • René Scalla, Michel Matringe, Jean-Michel Camadro, Pierre Labbe: Recent Advances in the Mode of Action of Diphenyl Ethers and Related Herbicides. In: Zeitschrift für Naturforschung C. Band 45, Nr. 5, 1. Mai 1990, S. 503–511, doi:10.1515/znc-1990-0535.
  • Stephen O. Duke, José M. Becerril, T. D. Sherman, John Lydon, Hiroshi Matsumoto: The role of protoporphyrin IX in the mechanism of action of diphenyl ether herbicides. In: Pesticide Science. Band 30, Nr. 4, 1990, S. 367–378, doi:10.1002/ps.2780300402.
  • Brighton Crop Protection Conference 1993 — Weeds: Introduction. In: Crop Protection. Band 12, Nr. 7, November 1993, S. 555–559, doi:10.1016/0261-2194(93)90101-n.
  • Clemens Lamberth, Andre Jeanguenat, Fredrik Cederbaum, Alain De Mesmaeker, Martin Zeller, Hans-Joachim Kempf, Ronald Zeun: Multicomponent reactions in fungicide research: The discovery of mandipropamid. In: Bioorganic & Medicinal Chemistry. Band 16, Nr. 3, 1. Februar 2008, S. 1531–1545, doi:10.1016/j.bmc.2007.10.019.
  • Yoshio Katsuda, Tadayoshi Chikamoto, Hiroshi Ogami, Hajime Hirobe, Tsutomu Kunishige: Novel Insecticidal Chrysanthemic Esters. In: Agricultural and Biological Chemistry. Band 33, Nr. 9, 1969, S. 1361–1362, doi:10.1271/bbb1961.33.1361.

drugbank.ca

europa.eu

echa.europa.eu

google.de

books.google.de

iupac.org

goldbook.iupac.org

  • The International Union of Pure and Applied Chemistry (IUPAC): acetylenes. In: iupac.org. goldbook.iupac.org, abgerufen am 21. Dezember 2023.
  • The International Union of Pure and Applied Chemistry (IUPAC): alkynes. In: iupac.org. goldbook.iupac.org, abgerufen am 21. Dezember 2023.

merckmillipore.com

nih.gov

ncbi.nlm.nih.gov

  • Robert E. Minto, Brenda J. Blacklock: Biosynthesis and function of polyacetylenes and allied natural products. In: Progress in Lipid Research. Band 47, Nr. 4, Juli 2008, S. 233–306, doi:10.1016/j.plipres.2008.02.002, PMID 18387369, PMC 2515280 (freier Volltext).
  • Qiu-Ye Chai, Zhen Yang, Hou-Wen Lin, Bing-Nan Han: Alkynyl-Containing Peptides of Marine Origin: A Review. In: Marine Drugs. Band 14, Nr. 11, 23. November 2016, S. 216, doi:10.3390/md14110216, PMID 27886049, PMC 5128759 (freier Volltext).
  • Douglass F. Taber, Sha Bai, Peng-fei Guo: A convenient reagent for aldehyde to alkyne homologation. In: Tetrahedron Letters. Band 49, Nr. 48, November 2008, S. 6904–6906, doi:10.1016/j.tetlet.2008.09.114, PMID 19946355, PMC 2634292 (freier Volltext).
  • Nabil Tahiri, Peter Fodran, Dhineshkumar Jayaraman, Jeffrey Buter, Martin D. Witte, Tonatiuh A. Ocampo, D. Branch Moody, Ildiko Van Rhijn, Adriaan J. Minnaard: Total Synthesis of a Mycolic Acid from Mycobacterium tuberculosis. In: Angewandte Chemie International Edition. Band 59, Nr. 19, 10. März 2020, S. 7555–7560, doi:10.1002/anie.202000523, PMID 32067294, PMC 7216993 (freier Volltext).
  • Siqi Zhang, Liang Zhao: A merged copper(I/II) cluster isolated from Glaser coupling. In: Nature Communications. Band 10, Nr. 1, 24. Oktober 2019, doi:10.1038/s41467-019-12889-w, PMID 31649254, PMC 6813345 (freier Volltext).
  • S. D. T. Maduwanthi, R. A. U. J. Marapana: Induced Ripening Agents and Their Effect on Fruit Quality of Banana. In: International Journal of Food Science. Band 2019, 2. Mai 2019, S. 1–8, doi:10.1155/2019/2520179, PMID 31187037, PMC 6521425 (freier Volltext).
  • Kusum V. Moray, Himanshu Chaurasia, Oshima Sachin, Beena Joshi: A systematic review on clinical effectiveness, side-effect profile and meta-analysis on continuation rate of etonogestrel contraceptive implant. In: Reproductive Health. Band 18, Nr. 1, Dezember 2021, doi:10.1186/s12978-020-01054-y, PMID 33407632, PMC 7788930 (freier Volltext).
  • Tamás Tábi, László Vécsei, Moussa B. Youdim, Peter Riederer, Éva Szökő: Selegiline: a molecule with innovative potential. In: Journal of Neural Transmission. Band 127, Nr. 5, Mai 2020, S. 831–842, doi:10.1007/s00702-019-02082-0, PMID 31562557, PMC 7242272 (freier Volltext).
  • Jin H. Park, Yingting Liu, Mark A. Lemmon, Ravi Radhakrishnan: Erlotinib binds both inactive and active conformations of the EGFR tyrosine kinase domain. In: Biochemical Journal. Band 448, Nr. 3, 15. Dezember 2012, S. 417–423, doi:10.1042/BJ20121513, PMID 23101586, PMC 3507260 (freier Volltext).
  • N. Spellmon, C. Li, Z. Yang: Allosterically targeting EGFR drug-resistance gatekeeper mutations. In: Journal of thoracic disease. Band 9, Nummer 7, Juli 2017, S. 1756–1758, doi:10.21037/jtd.2017.06.43, PMID 28839955, PMC 5542946 (freier Volltext).
  • Xiaohai Li, Theodore M. Kamenecka, Michael D. Cameron: Cytochrome P450-Mediated Bioactivation of the Epidermal Growth Factor Receptor Inhibitor Erlotinib to a Reactive Electrophile. In: Drug Metabolism and Disposition. Band 38, Nr. 7, Juli 2010, S. 1238–1245, doi:10.1124/dmd.109.030361, PMID 20382753, PMC 3202369 (freier Volltext).
  • Juliana T. W. Tong, Paul W. R. Harris, Margaret A. Brimble, Iman Kavianinia: An Insight into FDA Approved Antibody-Drug Conjugates for Cancer Therapy. In: Molecules. Band 26, Nr. 19, 27. September 2021, S. 5847, doi:10.3390/molecules26195847, PMID 34641391, PMC 8510272 (freier Volltext).
  • Gary S. Wood, Jianqiang Wu: Methotrexate and Pralatrexate. In: Dermatologic Clinics. Band 33, Nr. 4, Oktober 2015, S. 747–755, doi:10.1016/j.det.2015.05.009, PMID 26433846, PMC 5549926 (freier Volltext).
  • Julia Paik: Lenacapavir: First Approval. In: Drugs. Band 82, Nr. 14, September 2022, S. 1499–1504, doi:10.1007/s40265-022-01786-0, PMID 36272024, PMC 10267266 (freier Volltext).
  • L. C. Whelan, M. F. Ryan: Effects of the polyacetylene capillin on human tumour cell lines. In: Anticancer Research. Band 24, Nr. 4, 2004, S. 2281–2286, PMID 15330173.

pubchem.ncbi.nlm.nih.gov

nobelprize.org

wikidata.org