Wittig reaction (English Wikipedia)

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

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14doi.org

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3nih.gov

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doi.org

R. W. Hoffmann (2001). "Wittig and His Accomplishments: Still Relevant Beyond His 100th Birthday". Angewandte Chemie International Edition. 40 (8): 1411–1416. doi:10.1002/1521-3773(20010417)40:8<1411::AID-ANIE1411>3.0.CO;2-U. PMID 11317288.
E. Vedejs & C. F. Marth (1990). "Mechanism of Wittig reaction: evidence against betaine intermediates". J. Am. Chem. Soc. 112 (10): 3905–3909. doi:10.1021/ja00166a026.
E. Vedejs, C. F. Marth and R. Ruggeri (1988). "Substituent effects and the Wittig mechanism: the case of stereospecific oxaphosphetane decomposition". J. Am. Chem. Soc. 110 (12): 3940–48. doi:10.1021/ja00220a036.
E. Vedejs & C. F. Marth (1988). "Mechanism of the Wittig reaction: the role of substituents at phosphorus". J. Am. Chem. Soc. 110 (12): 3948–3958. doi:10.1021/ja00220a037.
Byrne, Peter A.; Gilheany, Declan G. (2013). "The modern interpretation of the Wittig reaction mechanism". Chemical Society Reviews. 42 (16): 6670–96. doi:10.1039/c3cs60105f. hdl:10197/4939. ISSN 0306-0012. PMID 23673458.
B. E. Maryanoff & A. B. Reitz (1989). "The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspects". Chem. Rev. 89 (4): 863–927. doi:10.1021/cr00094a007.
L. D. Bergelson & M. M. Shemyakin (1964). "Synthesis of Naturally Occurring Unsaturated Fatty Acids by Sterically Controlled Carbonyl Olefination". Angew. Chem. 3 (4): 250–260. doi:10.1002/anie.196402501.
Robiette, Raphaël; Richardson, Jeffery; Aggarwal, Varinder K.; Harvey, Jeremy N. (1 February 2006). "Reactivity and Selectivity in the Wittig Reaction: A Computational Study". Journal of the American Chemical Society. 128 (7): 2394–2409. doi:10.1021/ja056650q. ISSN 0002-7863. PMID 16478195.
M. Schlosser & K. F. Christmann (1966). "Trans-Selective Olefin Syntheses". Angewandte Chemie International Edition in English. 5 (1): 126. doi:10.1002/anie.196601261.
E. J. Corey and H. Yamamoto (1970). "Modification of the Wittig reaction to permit the stereospecific synthesis of certain trisubstituted olefins. Stereospecific synthesis of α-santalol". J. Am. Chem. Soc. 92 (1): 226–228. doi:10.1021/ja00704a052.
I. Ernest, A. J. Main and R. Menasse (1982). "Synthesis of the 7-cis isomer of the natural leukotriene d₄". Tetrahedron Letters. 23 (2): 167–170. doi:10.1016/S0040-4039(00)86776-3.
E. J. Corey, D. A. Clark, G. Goto, A. Marfat, C. Mioskowski, B. Samuelsson and S. Hammarstroem (1980). "Stereospecific total synthesis of a "slow reacting substance" of anaphylaxis, leukotriene C-1". J. Am. Chem. Soc. 102 (4): 1436–1439. doi:10.1021/ja00524a045.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Georg Wittig, Ulrich Schöllkopf (1954). "Über Triphenyl-phosphin-methylene als olefinbildende Reagenzien I". Chemische Berichte. 87 (9): 1318. doi:10.1002/cber.19540870919.
Georg Wittig; Werner Haag (1955). "Über Triphenyl-phosphin-methylene als olefinbildende Reagenzien II". Chemische Berichte. 88 (11): 1654–1666. doi:10.1002/cber.19550881110.

handle.net

hdl.handle.net

Byrne, Peter A.; Gilheany, Declan G. (2013). "The modern interpretation of the Wittig reaction mechanism". Chemical Society Reviews. 42 (16): 6670–96. doi:10.1039/c3cs60105f. hdl:10197/4939. ISSN 0306-0012. PMID 23673458.

nih.gov

pubmed.ncbi.nlm.nih.gov

R. W. Hoffmann (2001). "Wittig and His Accomplishments: Still Relevant Beyond His 100th Birthday". Angewandte Chemie International Edition. 40 (8): 1411–1416. doi:10.1002/1521-3773(20010417)40:8<1411::AID-ANIE1411>3.0.CO;2-U. PMID 11317288.
Byrne, Peter A.; Gilheany, Declan G. (2013). "The modern interpretation of the Wittig reaction mechanism". Chemical Society Reviews. 42 (16): 6670–96. doi:10.1039/c3cs60105f. hdl:10197/4939. ISSN 0306-0012. PMID 23673458.
Robiette, Raphaël; Richardson, Jeffery; Aggarwal, Varinder K.; Harvey, Jeremy N. (1 February 2006). "Reactivity and Selectivity in the Wittig Reaction: A Computational Study". Journal of the American Chemical Society. 128 (7): 2394–2409. doi:10.1021/ja056650q. ISSN 0002-7863. PMID 16478195.

orgsyn.org

Richard J. K. Taylor, Leonie Campbell, and Graeme D. McAllister (2008). "(±) trans-3,3'-(1,2-Cyclopropanediyl)bis-2-(E)-propenoic Acid, Diethyl Ester: Tandem Oxidation Procedure (TOP) using MnO₂ Oxidation-Stabilized Phosphorane Trapping" (PDF). Organic Syntheses. 85: 15–26{{cite journal}}: CS1 maint: multiple names: authors list (link).

worldcat.org

Byrne, Peter A.; Gilheany, Declan G. (2013). "The modern interpretation of the Wittig reaction mechanism". Chemical Society Reviews. 42 (16): 6670–96. doi:10.1039/c3cs60105f. hdl:10197/4939. ISSN 0306-0012. PMID 23673458.
Robiette, Raphaël; Richardson, Jeffery; Aggarwal, Varinder K.; Harvey, Jeremy N. (1 February 2006). "Reactivity and Selectivity in the Wittig Reaction: A Computational Study". Journal of the American Chemical Society. 128 (7): 2394–2409. doi:10.1021/ja056650q. ISSN 0002-7863. PMID 16478195.