Oliver P. Ernst, David T. Lodowski, Marcus Elstner, Peter Hegemann, Leonid S. Brown, Hideki Kandori: Microbial and Animal Rhodopsins: Structures, Functions, and Molecular Mechanisms. In: Chemical Reviews. Band114, Nr.1, 8. Januar 2014, S.126–163, doi:10.1021/cr4003769, PMID 24364740, PMC 3979449 (freier Volltext) – (acs.org [abgerufen am 20. Oktober 2024]).
books.google.com
Ludwig Acker, Gerhard Bressau, Georg Benedikt Brubacher, Karl Maximilian Bürger, Stefan Diemair, Willibald Diemair, Klaus Doerffel, Rudi Franck, Hansfriedel Gudjons, Paul Joppien, Ludwig Kotter, Ernst Kröller, Hermvn Libert, Helmut Mühlschlegel, Titus Niedermaier, Konrad Pfeilsticker, Gerhard Pfleiderer, Wilhelm Postel, Hanspeter P. Probst, W. Rödder, Werner Schäfer, Leopold Schmid, Erich Schneider, Artur Seher, Hans Sommer, Helmut Thaler, Jean Paul Vuilleumier, Herbert Woidich: Analytik der Lebensmittel Nachweis und Bestimmung von Lebensmittel-Inhaltsstoffen. Springer-Verlag, 2013, ISBN 978-3-642-46069-2, S.648 (books.google.com).
Ira Remsen: Justus von Liebig, His Life and Work (1803-1873). By W. A. Shenstone, F. I. C., Lecturer on Chemistry in Clifton College. New York, Macmillan & Co. 1895. Pp. 220 + vi. In: Science. Band3, Nr.53, 3. Januar 1896, S.62–63, doi:10.1126/science.3.53.24.
Holde Puchtler, Susan N. Meloan, Barbara R. Brewton: On the history of basic fuchsin and aldehyde-schiff reactions from 1862 to 1935. In: Histochemistry. Band41, Nr.3, 1975, S.185–194, doi:10.1007/BF00497682.
Chérifa Boulechfar, Hana Ferkous, Amel Delimi, Amel Djedouani, Abdesalem Kahlouche, Abir Boublia, Ahmad S. Darwish, Tarek Lemaoui, Rajesh Verma, Yacine Benguerba: Schiff bases and their metal Complexes: A review on the history, synthesis, and applications. In: Inorganic Chemistry Communications. Band150, April 2023, S.110451, doi:10.1016/j.inoche.2023.110451.
The IUPAC Compendium of Chemical Terminology: The Gold Book. 4. Auflage. International Union of Pure and Applied Chemistry (IUPAC), Research Triangle Park, NC 2019, doi:10.1351/goldbook.a00208.
The IUPAC Compendium of Chemical Terminology: The Gold Book. 4. Auflage. International Union of Pure and Applied Chemistry (IUPAC), Research Triangle Park, NC 2019, doi:10.1351/goldbook.k03386.
Mikko Salaspuro: Acetaldehyde and gastric cancer. In: Journal of Digestive Diseases. Band12, Nr.2, April 2011, S.51–59, doi:10.1111/j.1751-2980.2011.00480.x.
Oliver P. Ernst, David T. Lodowski, Marcus Elstner, Peter Hegemann, Leonid S. Brown, Hideki Kandori: Microbial and Animal Rhodopsins: Structures, Functions, and Molecular Mechanisms. In: Chemical Reviews. Band114, Nr.1, 8. Januar 2014, S.126–163, doi:10.1021/cr4003769, PMID 24364740, PMC 3979449 (freier Volltext) – (acs.org [abgerufen am 20. Oktober 2024]).
Claus Wasternack: Oxylipins: Biosynthesis, Signal Transduction and Action. In: Annual Plant Reviews Volume 24: Plant Hormone Signaling. 1. Auflage. Wiley, 2006, ISBN 978-1-4051-3887-1, S.189–192, doi:10.1002/9780470988800.ch7.
Kenji Matsui: Green leaf volatiles: hydroperoxide lyase pathway of oxylipin metabolism. In: Current Opinion in Plant Biology. Band9, Nr.3, Juni 2006, S.274–280, doi:10.1016/j.pbi.2006.03.002.
Nicholas J. Lawrence: Aldehydes and ketones. In: Journal of the Chemical Society, Perkin Transactions 1. Nr.10, 1998, S.1739–1750, doi:10.1039/a800646f.
Sivaraman Balasubramaniam, Indrapal Aidhen: The Growing Synthetic Utility of the Weinreb Amide. In: Synthesis. Band2008, Nr.23, Dezember 2008, S.3707–3738, doi:10.1055/s-0028-1083226.
S. Chandrasekhar, M. Suresh Kumar, B. Muralidhar: One pot conversion of car☐ylic acids to aldehydes with DIBAL-H. In: Tetrahedron Letters. Band39, Nr.8, Februar 1998, S.909–910, doi:10.1016/S0040-4039(97)10688-8.
Siegfried R. Waldvogel: Strategic Applications of Named Reactions in Organic Synthesis. Background and Detailed Mechanisms. By Laszlo Kürti and Barbara Czako. In: Angewandte Chemie International Edition. Band44, Nr.32, 12. August 2005, S.5005–5006, doi:10.1002/anie.200585304.
Elias J. Corey, Norman W. Gilman, B. E. Ganem: New methods for the oxidation of aldehydes to carboxylic acids and esters. In: Journal of the American Chemical Society. Band90, Nr.20, September 1968, S.5616–5617, doi:10.1021/ja01022a059.
Liyuan Lan, Shuai Huang, Yongguo Liu, Baoguo Sun, Hongyu Tian: Preparation and odor characteristics of nitriles derived from aldehydes. In: Flavour and Fragrance Journal. Band35, Nr.4, Juli 2020, S.425–434, doi:10.1002/ffj.3581.
Dylan J. Quinn, Graham J. Haun, Gustavo Moura-Letts: Direct synthesis of nitriles from aldehydes with hydroxylamine-O-sulfonic acid in acidic water. In: Tetrahedron Letters. Band57, Nr.34, August 2016, S.3844–3847, doi:10.1016/j.tetlet.2016.07.047.
Antonella Leggio, Emilia Lucia Belsito, Sonia Gallo, Angelo Liguori: One-pot conversion of aldehydes to nitriles mediated by TiCl 4. In: Tetrahedron Letters. Band58, Nr.15, April 2017, S.1512–1514, doi:10.1016/j.tetlet.2017.03.007.
Cheves. Walling, Michael J. Mintz: Positive Halogen Compounds. XIII. t-Butyl Hypochlorite Chlorination of Ethers, Aldehydes, and Other Molecules with Polar Substituents. In: Journal of the American Chemical Society. Band89, Nr.6, März 1967, S.1515–1519, doi:10.1021/ja00982a040.
Nitin D. Arote, Krishnacharya G. Akamanchi: Direct conversion of aldehydes to acyl azides using tert-butyl hypochlorite. In: Tetrahedron Letters. Band48, Nr.32, August 2007, S.5661–5664, doi:10.1016/j.tetlet.2007.06.020.
Robert F. Nystrom, Weldon G. Brown: Reduction of Organic Compounds by Lithium Aluminum Hydride. I. Aldehydes, Ketones, Esters, Acid Chlorides and Acid Anhydrides. In: Journal of the American Chemical Society. Band69, Nr.5, Mai 1947, S.1197–1199, doi:10.1021/ja01197a060.
Mathias Glatz, Berthold Stöger, Daniel Himmelbauer, Luis F. Veiros, Karl Kirchner: Chemoselective Hydrogenation of Aldehydes under Mild, Base-Free Conditions: Manganese Outperforms Rhenium. In: ACS Catalysis. Band8, Nr.5, 4. Mai 2018, S.4009–4016, doi:10.1021/acscatal.8b00153, PMID 29755828, PMC 5939901 (freier Volltext).
C. W. Jung, P. E. Garrou: Dehydrogenation of alcohols and hydrogenation of aldehydes using homogeneous ruthenium catalysts. In: Organometallics. Band1, Nr.4, April 1982, S.658–666, doi:10.1021/om00064a016.
A. L. Wilds: Reduction with Aluminum Alkoxides. In: Organic Reactions. 15. März 2011, S.179–180, doi:10.1002/0471264180.or002.05.
David Kieslich, Jens Christoffers: Cyanide Anions as Nucleophilic Catalysts in Organic Synthesis. In: Synthesis. Band53, Nr.19, Oktober 2021, S.3485–3496, doi:10.1055/a-1499-8943.
Guangkuan Zhao, Ling‐Zhi Yuan, Mouad Alami, Olivier Provot: Desulfurization of Thioketals into Methylene and Methyl Derivatives: Nickel or not Nickel? In: ChemistrySelect. Band2, Nr.33, 21. November 2017, S.10951–10959, doi:10.1002/slct.201702370.
Bo Han, Chunping Ren, Min Jiang, Lipeng Wu: Titanium‐Catalyzed Exhaustive Reduction of Oxo‐Chemicals. In: Angewandte Chemie International Edition. Band61, Nr.46, 14. November 2022, doi:10.1002/anie.202209232.
Christopher M. Beck, Scott E. Rathmill, You Jung Park, Junyi Chen, Robert H. Crabtree, Louise M. Liable-Sands, Arnold L. Rheingold: Aldehyde Decarbonylation Catalysis under Mild Conditions. In: Organometallics. Band18, Nr.25, 1. Dezember 1999, S.5311–5317, doi:10.1021/om9905106.
Ian Beadham, Jason Micklefield: Reagents for Carbonyl Methylenation in Organic Synthesis. In: Current Organic Synthesis. Band2, Nr.2, S.231–259, doi:10.2174/1570179053545396.
Bernhard Breit: Dithioacetals as an Entry to Titanium-Alkylidene Chemistry: A New and Efficient Carbonyl Olefination. In: Angewandte Chemie International Edition. Band37, Nr.4, 2. März 1998, S.453–456, doi:10.1002/(SICI)1521-3773(19980302)37:4<453::AID-ANIE453>3.0.CO;2-M.
Damien Habrant, Vesa Rauhala, Ari M. P. Koskinen: Conversion of carbonyl compounds to alkynes: general overview and recent developments. In: Chemical Society Reviews. Band39, Nr.6, 2010, S.2007, doi:10.1039/b915418c.
E.J. Corey, P.L. Fuchs: A synthetic method for formyl→ethynyl conversion (RCHO→RCCH or RCCR′). In: Tetrahedron Letters. Band13, 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. Band2000, Nr.02, 2000, S.185–213, doi:10.1055/s-2000-6241.
Sabine Bognar, Manuel van Gemmeren: Direct Synthesis of Unsymmetrical Dithioacetals. In: Chemistry – A European Journal. Band27, Nr.15, 12. März 2021, S.4859–4863, doi:10.1002/chem.202004835, PMID 33270274, PMC 8048688 (freier Volltext).
Walter M. Lauer, Carl M. Langkammerer: The Constitution of the Bisulfite Addition Compounds of Aldehydes and Ketones. In: Journal of the American Chemical Society. Band57, Nr.12, Dezember 1935, S.2360–2362, doi:10.1021/ja01315a007.
Robert J. H. Gregory: Cyanohydrins in Nature and the Laboratory: Biology, Preparations, and Synthetic Applications. In: Chemical Reviews. Band99, Nr.12, 8. Dezember 1999, S.3649–3682, doi:10.1021/cr9902906.
Hiroshi Ohno, Atsunori Mori, Shohei Inoue: Lanthanoid(III) Alkoxides as Novel Catalysts for a Rapid Transhydrocyanation from Acetone Cyanohydrin to Aldehydes and Ketones. In: Chemistry Letters. Band22, Nr.2, 1. Februar 1993, S.375–378, doi:10.1246/cl.1993.375.
Wayiza Masamba: Petasis vs. Strecker Amino Acid Synthesis: Convergence, Divergence and Opportunities in Organic Synthesis. In: Molecules. Band26, Nr.6, 18. März 2021, S.1707, doi:10.3390/molecules26061707, PMID 33803879, PMC 8003338 (freier Volltext).
M. S. Peters, J. A. Quinn: Pentaerythritol Production Yields. In: Industrial & Engineering Chemistry. Band47, Nr.9, September 1955, S.1710–1713, doi:10.1021/ie50549a016.
David E. Lewis: Aleksei Yevgen'evich Chichibabin (1871–1945): A Century of Pyridine Chemistry. In: Angewandte Chemie International Edition. Band56, Nr.33, 7. August 2017, S.9660–9668, doi:10.1002/anie.201611724.
Adam W. Franz, Helmut Kronemayer, Daniel Pfeiffer, Roman D. Pilz, Günther Reuss, Walter Disteldorf, Armin Otto Gamer, Albrecht Hilt: Formaldehyde. In: Ullmann's Encyclopedia of Industrial Chemistry. Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, Germany 2016, ISBN 978-3-527-30673-2, S.1–34, doi:10.1002/14356007.a11_619.pub2.
Sandro Nalli, Owen J. Horn, Adam R. Grochowalski, David G. Cooper, Jim A. Nicell: Origin of 2-ethylhexanol as a VOC. In: Environmental Pollution. Band140, Nr.1, März 2006, S.181–185, doi:10.1016/j.envpol.2005.06.018.
Thomas Willke: Methionine production—a critical review. In: Applied Microbiology and Biotechnology. Band98, Nr.24, Dezember 2014, S.9893–9914, doi:10.1007/s00253-014-6156-y.
A Nuryawan, I Risnasari, T Sucipto, A Heri Iswanto, R Rosmala Dewi: Urea-formaldehyde resins: production, application, and testing. In: IOP Conference Series: Materials Science and Engineering. Band223, Juli 2017, S.012053, doi:10.1088/1757-899X/223/1/012053.
Alexander T. Cartus, Dirk W. Lachenmeier, Sabine Guth, Angelika Roth, Matthias Baum, Patrick Diel, Gerhard Eisenbrand, Barbara Engeli, Michael Hellwig, Hans‐Ulrich Humpf, Hans‐Georg Joost, Sabine E. Kulling, Alfonso Lampen, Doris Marko, Pablo Steinberg, Wim Wätjen, Jan G. Hengstler, Angela Mally: Acetaldehyde as a Food Flavoring Substance: Aspects of Risk Assessment. In: Molecular Nutrition & Food Research. Band67, Nr.23, Dezember 2023, doi:10.1002/mnfr.202200661.
Anton C. De Groot, Margo Veenstra: Formaldehyde‐releasers in cosmetics in the USA and in Europe. In: Contact Dermatitis. Band62, Nr.4, April 2010, S.221–224, doi:10.1111/j.1600-0536.2009.01623.x.
Rooban Thavarajah, VidyaKazhiyur Mudimbaimannar, Joshua Elizabeth, UmadeviKrishnamohan Rao, Kannan Ranganathan: Chemical and physical basics of routine formaldehyde fixation. In: Journal of Oral and Maxillofacial Pathology. Band16, Nr.3, 2012, S.400, doi:10.4103/0973-029X.102496, PMID 23248474, PMC 3519217 (freier Volltext).
Willi Melber, Peter Böhm: Einführung in die Nomenklatur organisch-chemischer Verbindungen für Studium und Berufsausbildung. Springer Berlin Heidelberg, 1987, ISBN 3-642-93370-X, S.75 (eingeschränkte Vorschau in der Google-Buchsuche).
Adalbert Wollrab: Organische Chemie Eine Einführung für Lehramts- und Nebenfachstudenten. Springer-Verlag, 2013, ISBN 978-3-662-09137-1, S.402ff. (eingeschränkte Vorschau in der Google-Buchsuche).
Andrew Burrows, John Holman, Simon Lancaster, Andrew Parsons, Tina Overton, Gwen Pilling, Gareth Price: Chemistry3. Oxford University Press, 2021, ISBN 978-0-19-882998-0, S.1059 (eingeschränkte Vorschau in der Google-Buchsuche).
P. Tharmaraj, J. Shakina, R. Sujatha, L. Alphonse: Green Chemistry. AG PUBLISHING HOUSE (AGPH Books), ISBN 978-81-19-15262-9, S.113 (eingeschränkte Vorschau in der Google-Buchsuche).
Stefanie Federle, Stefanie Hergesell, Sebastian Schubert: Die Stoffklassen der organischen Chemie. Springer Berlin Heidelberg, 2017, ISBN 978-3-662-54968-1, S.186 (eingeschränkte Vorschau in der Google-Buchsuche).
nih.gov
ncbi.nlm.nih.gov
Oliver P. Ernst, David T. Lodowski, Marcus Elstner, Peter Hegemann, Leonid S. Brown, Hideki Kandori: Microbial and Animal Rhodopsins: Structures, Functions, and Molecular Mechanisms. In: Chemical Reviews. Band114, Nr.1, 8. Januar 2014, S.126–163, doi:10.1021/cr4003769, PMID 24364740, PMC 3979449 (freier Volltext) – (acs.org [abgerufen am 20. Oktober 2024]).
Mathias Glatz, Berthold Stöger, Daniel Himmelbauer, Luis F. Veiros, Karl Kirchner: Chemoselective Hydrogenation of Aldehydes under Mild, Base-Free Conditions: Manganese Outperforms Rhenium. In: ACS Catalysis. Band8, Nr.5, 4. Mai 2018, S.4009–4016, doi:10.1021/acscatal.8b00153, PMID 29755828, PMC 5939901 (freier Volltext).
Sabine Bognar, Manuel van Gemmeren: Direct Synthesis of Unsymmetrical Dithioacetals. In: Chemistry – A European Journal. Band27, Nr.15, 12. März 2021, S.4859–4863, doi:10.1002/chem.202004835, PMID 33270274, PMC 8048688 (freier Volltext).
Wayiza Masamba: Petasis vs. Strecker Amino Acid Synthesis: Convergence, Divergence and Opportunities in Organic Synthesis. In: Molecules. Band26, Nr.6, 18. März 2021, S.1707, doi:10.3390/molecules26061707, PMID 33803879, PMC 8003338 (freier Volltext).
Rooban Thavarajah, VidyaKazhiyur Mudimbaimannar, Joshua Elizabeth, UmadeviKrishnamohan Rao, Kannan Ranganathan: Chemical and physical basics of routine formaldehyde fixation. In: Journal of Oral and Maxillofacial Pathology. Band16, Nr.3, 2012, S.400, doi:10.4103/0973-029X.102496, PMID 23248474, PMC 3519217 (freier Volltext).
spektrum.de
Ameisensäure. In: Spektrum.de Lexikon der Chemie. Abgerufen am 5. Juni 2024.
