Literature DB >> 15571380

Stannylative cycloaddition of enynes catalyzed by palladium-iminophosphine.

Yoshiaki Nakao1, Yasuhiro Hirata, Shinjiro Ishihara, Shinichi Oda, Tomoya Yukawa, Eiji Shirakawa, Tamejiro Hiyama.   

Abstract

Palladium-iminophosphine complex catalyzes stannylative cycloaddition of conjugated enynes using hexabutyldistannoxane as a stannylating agent to afford highly substituted 3-alkenylphenylstannanes regioselectively. Stannylative cross-cycloaddition reactions between different enynes or between enynes and diynes are also achieved. The reaction is successfully applied to a concise synthesis of alcyopterosin N, which has been isolated recently from sub-Antarctic soft coral, Alcyonium paessleri.

Entities:  

Year:  2004        PMID: 15571380     DOI: 10.1021/ja044429s

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  1 in total

Review 1.  Secondary Metabolites from Polar Organisms.

Authors:  Yuan Tian; Yan-Ling Li; Feng-Chun Zhao
Journal:  Mar Drugs       Date:  2017-02-23       Impact factor: 5.118

  1 in total

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