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Aryne (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Aryne" in English language version.

refsWebsite
Global rank English rank
36doi.org
2nd place
2nd place
15nih.gov
4th place
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5harvard.edu
18th place
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3iupac.org
538th place
863rd place
2worldcat.org
5th place
5th place
1archive.org
6th place
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1orgsyn.org
2,971st place
2,826th place
1zenodo.org
621st place
380th place
1semanticscholar.org
11th place
8th place

archive.org

doi.org

  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Aryne". doi:10.1351/goldbook.A00465
  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Benzynes". doi:10.1351/goldbook.B00634
  • Hans Henning Wenk; Michael Winkler; Wolfram Sander (2003). "One Century of Aryne Chemistry". Angew. Chem. Int. Ed. 42 (5): 502–528. doi:10.1002/anie.200390151. PMID 12569480.
  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Dehydroarenes". doi:10.1351/goldbook.D01574
  • Gampe, C. M.; Carreira, E. M. (2012). "Arynes and Cyclohexyne in Natural Product Synthesis". Angew. Chem. Int. Ed. Engl. 51 (16): 3766–78. doi:10.1002/anie.201107485. PMID 22422638.
  • Radziszewski, J. G.; Hess, B. A. Jr.; Zahradnik, R. (1992). "Infrared Spectrum of o-Benzyne: Experiment and Theory". J. Am. Chem. Soc. 114: 52. doi:10.1021/ja00027a007.
  • Hoffmann, R.; Imamura, A.; Hehre, W. J. (1968). "Benzynes, dehydroconjugated molecules, and the interaction of orbitals separated by a number of intervening sigma bonds". J. Am. Chem. Soc. 90 (6): 1499. doi:10.1021/ja01008a018.
  • Wittig, Georg (1959). "Triptycene". Org. Synth. 39: 75. doi:10.15227/orgsyn.039.0075.
  • Sullivan, John M. (1971-06-01). "Explosion during preparation of benzenediazonium-2-carboxylate hydrochloride". Journal of Chemical Education. 48 (6): 419. Bibcode:1971JChEd..48..419S. doi:10.1021/ed048p419.3. ISSN 0021-9584.
  • Logullo, Francis M.; Seitz, Arnold M.; Friedman, Lester (1968). "Benzenediazonium-2-Carboxylate and Biphenylene (Benzenediazonium, o-carboxy-, hydroxide, inner salt)". Org. Synth. 48: 12. doi:10.15227/orgsyn.048.0012.
  • Tadross, P. M.; Stoltz, B. M. (2012). "A Comprehensive History of Arynes in Natural Product Total Synthesis". Chem. Rev. 112 (6): 3550–3577. doi:10.1021/cr200478h. PMID 22443517.
  • Hoye, T. R.; Baire, B.; Niu, D.; Willoughby, P. H.; Woods, B. P. (2012). "The hexadehydro-Diels–Alder reaction". Nature. 490 (7419): 208–212. Bibcode:2012Natur.490..208H. doi:10.1038/nature11518. PMC 3538845. PMID 23060191.
  • Campbell, C.D.; C.W. Rees (1969). "Reactive intermediates. Part I. Synthesis and oxidation of 1- and 2-aminobenzotriazole". J. Chem. Soc. C. 1969 (5): 742–747. doi:10.1039/J39690000742.
  • Mizukoshi, Yoshihide; Mikami, Koichiro; Uchiyama, Masanobu (2015). "Aryne Polymerization Enabling Straightforward Synthesis of Elusive Poly(ortho-arylene)s". J. Am. Chem. Soc. 137 (1): 74–77. doi:10.1021/ja5112207. PMID 25459083.
  • "1,2,3,4-Tetraphenylnaphthalene". Organic Syntheses. 46: 107. 1966. doi:10.15227/orgsyn.046.0107.
  • "Use of 1,2,4,5-Tetrabromobenzene as a 1,4-Nenzadiyne Equivalent: Anti- and Syn-1,4,5,8-tetrahydroanthracene 1,4:5,8-diepoxides". Organic Syntheses. 75: 201. 1998. doi:10.15227/orgsyn.075.0201.
  • Buszek, K. R.; Brown, N.; Kuo, D. (2009). "Concise Total Synthesis of (±)-cis-Trikentrin A and (±)-Herbindole A via Intermolecular Indole Aryne Cycloaddition". Org. Lett. 11 (1): 201–204. doi:10.1021/ol802425m. PMC 2723800. PMID 19055375.
  • Blake, M. E.; Bartlett, K. L.; Jones, M. Jr (2003). "A m-Benzyne to o-Benzyne Conversion Through a 1,2-Shift of a Phenyl Group". J. Am. Chem. Soc. 125 (21): 6485–90. doi:10.1021/ja0213672. PMID 12785789.
  • Polishchuk, A. L.; Bartlett, K. L.; Friedman, L. A.; Jones, M. Jr (2004). "A p-Benzyne to m-Benzyne Conversion Through a 1,2-Shift of a Phenyl Group. Completion of the Benzyne Cascade". J. Phys. Org. Chem. 17 (9): 798–806. doi:10.1002/poc.797.
  • Richard R. Jones; Robert G. Bergman (1972). "p-Benzyne. Generation as an intermediate in a thermal isomerization reaction and trapping evidence for the 1,4-benzenediyl structure". J. Am. Chem. Soc. 94 (2): 660–661. doi:10.1021/ja00757a071.
  • Clauberg, H.; Minsek, D. W.; Chen, P. (1992). "Mass and photoelectron spectroscopy of C3H2. .DELTA.Hf of singlet carbenes deviate from additivity by their singlet-triplet gaps". J. Am. Chem. Soc. 114: 99. doi:10.1021/ja00027a014.
  • Blush, J. A.; Clauberg, H.; Kohn, D. W.; Minsek, D. W.; Zhang, X.; Chen, P. (1992). "Photoionization mass and photoelectron spectroscopy of radicals, carbenes, and biradicals". Acc. Chem. Res. 25 (9): 385. doi:10.1021/ar00021a001.
  • Chen, P (1996). "Design of Diradical-based Hydrogen Abstraction Agents". Angew. Chem. Int. Ed. Engl. 35 (1314): 1478. doi:10.1002/anie.199614781.
  • Stoermer, R.; Kahlert, B. (1902). "Ueber das 1- und 2-Brom-cumaron". Berichte der Deutschen Chemischen Gesellschaft. 35 (2): 1633–1640. doi:10.1002/cber.19020350286.
  • Wittig, G.; Pieper, G.; Fuhrmann, G. (1940). "Über die Bildung von Diphenyl aus Fluorbenzol und Phenyl-lithium (IV. Mitteil. über Austauschreaktionen mit Phenyl-lithium)". Berichte der Deutschen Chemischen Gesellschaft (A and B Series). 73 (11): 1193–1197. doi:10.1002/cber.19400731113.
  • Wittig, Georg (1942). "Phenyl-lithium, der Schlüssel zu einer neuen Chemie metallorganischer Verbindungen". Die Naturwissenschaften. 30 (46–47): 696–703. Bibcode:1942NW.....30..696W. doi:10.1007/BF01489519. S2CID 37148502.
  • Wittig, G (1954). "Fortschritte auf dem Gebiet der organischen Aniono-Chemie". Angewandte Chemie. 66 (1): 10–17. Bibcode:1954AngCh..66...10W. doi:10.1002/ange.19540660103.
  • Roberts, John D. (1953). "Rearrangement in the Reaction of Chlorobenzene-1-C14With Potassium Amide1". Journal of the American Chemical Society. 75 (13): 3290–3291. doi:10.1021/ja01109a523.
  • Roberts, John D. (1956). "The Mechanism of Aminations of Halobenzenes 1". Journal of the American Chemical Society. 78 (3): 601–611. doi:10.1021/ja01584a024.
  • Roberts, John D. (1956). "Orientation in Aminations of Substituted Halobenzenes 1". Journal of the American Chemical Society. 78 (3): 611–614. doi:10.1021/ja01584a025.
  • Heaney, H. (1962). "The Benzyne and Related Intermediates". Chemical Reviews. 62 (2): 81–97. doi:10.1021/cr60216a001.
  • Warmuth, R.; Yoon (2001). "Recent highlights in hemicarcerand chemistry". Acc. Chem. Res. 34 (2): 96. doi:10.1021/ar980082k. PMID 11263868.
  • On-surface; Pérez, E.Guitián; Peña, L.Gross (2015). "On-surface generation and imaging of arynes by atomic force microscopy". Nature Chemistry. 7 (8): 623–8. Bibcode:2015NatCh...7..623P. doi:10.1038/nchem.2300. PMID 26201737.
  • Galm, U; Hager, MH; Van Lanen, SG; Ju, J; Thorson, JS; Shen, B (Feb 2005). "Antitumor antibiotics: bleomycin, enediynes, and mitomycin". Chemical Reviews. 105 (2): 739–58. doi:10.1021/cr030117g. PMID 15700963.
  • Day, J. J.; McFadden, R. M.; Virgil, S. C.; Kolding, H.; Alleva, J. L.; Stoltz, B. M. (2011). "The catalytic enantioselective total synthesis of (+)-liphagal". Angew. Chem. Int. Ed. 50 (30): 6814–8. doi:10.1002/anie.201101842. PMC 3361906. PMID 21671325.
  • Soorukram, D.; Qu, T.; Barrett, A. G. M. (2008). "Four-Component Benzyne Coupling Reactions: A Concise Total Synthesis of Dehydroaltenuene B". Org. Lett. 10 (17): 3833–3835. doi:10.1021/ol8015435. PMID 18672878.

harvard.edu

ui.adsabs.harvard.edu

iupac.org

goldbook.iupac.org

  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Aryne". doi:10.1351/goldbook.A00465
  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Benzynes". doi:10.1351/goldbook.B00634
  • IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version: (2006–) "Dehydroarenes". doi:10.1351/goldbook.D01574

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

orgsyn.org

semanticscholar.org

api.semanticscholar.org

worldcat.org

zenodo.org