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A Novel Method for the Stereoselective Synthesis of trans Olefins

1974; Wiley; Volume: 13; Issue: 6 Linguagem: Inglês

10.1002/anie.197404071

1521-3773

Kiyosi Kondô, Akira Negishi, Daiei Tunemoto,

Asymmetric Synthesis and Catalysis

Angewandte Chemie International Edition in EnglishVolume 13, Issue 6 p. 407-408 Communication A Novel Method for the Stereoselective Synthesis of trans Olefins Dr. Kiyosi Kondo, Corresponding Author Dr. Kiyosi Kondo Sagami Chemical Research Center 4-4-1, Nishionuma, Sagamihara Kanagawa, 229 (Japan)Sagami Chemical Research Center 4-4-1, Nishionuma, Sagamihara Kanagawa, 229 (Japan)Search for more papers by this authorDr. Akira Negishi, Dr. Akira Negishi Sagami Chemical Research Center 4-4-1, Nishionuma, Sagamihara Kanagawa, 229 (Japan)Search for more papers by this authorDipl.-Chem. Daiei Tunemoto, Dipl.-Chem. Daiei Tunemoto Sagami Chemical Research Center 4-4-1, Nishionuma, Sagamihara Kanagawa, 229 (Japan)Search for more papers by this author Dr. Kiyosi Kondo, Corresponding Author Dr. Kiyosi Kondo Sagami Chemical Research Center 4-4-1, Nishionuma, Sagamihara Kanagawa, 229 (Japan)Sagami Chemical Research Center 4-4-1, Nishionuma, Sagamihara Kanagawa, 229 (Japan)Search for more papers by this authorDr. Akira Negishi, Dr. Akira Negishi Sagami Chemical Research Center 4-4-1, Nishionuma, Sagamihara Kanagawa, 229 (Japan)Search for more papers by this authorDipl.-Chem. Daiei Tunemoto, Dipl.-Chem. Daiei Tunemoto Sagami Chemical Research Center 4-4-1, Nishionuma, Sagamihara Kanagawa, 229 (Japan)Search for more papers by this author First published: June 1974 https://doi.org/10.1002/anie.197404071Citations: 36AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. References 1 G. Lavielle, C. R. Acad. Sci. C 270, 86 (1970). CASWeb of Science®Google Scholar 2 E. J. Corey and G. T. Kwiatkowski, J. Amer. Chem. Soc. 88, 5654 (1966). 10.1021/ja00975a057 CASWeb of Science®Google Scholar 3 J. Reucroft and P. G. Sammes, Quart. Rev. Chem. Soc. 25, 135 (1971), and references cited therein. 10.1039/qr9712500135 CASGoogle Scholar 4 P. Vittorelli, T. Winkler, H. J. Hansen, and H. Schmid, Helv. Chim. Acta 51, 1457 (1968). 10.1002/hlca.19680510631 CASWeb of Science®Google Scholar 5 J. Weatherston, W. Roelofs, A. Comeau, and C. J. Sanders, Can. Entomol. 103, 1741 (1971). 10.4039/Ent1031741-12 CASWeb of Science®Google Scholar 6 F. L. M. Pattisan, J. B. Stothers, and R. G. Woolford, J. Amer. Chem. Soc. 78, 2255 (1956). 10.1021/ja01591a062 Google Scholar Citing Literature Volume13, Issue6June 1974Pages 407-408 ReferencesRelatedInformation