Literature DB >> 15012068

A highly regio- and stereoselective carbocupration of fluoroalkylated internal alkynes: a short total synthesis of the antiestrogenic drug panomifene.

Tsutomu Konno1, Takeshi Daitoh, Atsushi Noiri, Jungha Chae, Takashi Ishihara, Hiroki Yamanaka.   

Abstract

[reaction: see text] A highly regio- and stereoselective carbometalation reaction of fluoroalkylated internal alkynes with organocopper reagents is described. This reaction is utilized successfully in the short, stereoselective total synthesis of the antiestrogenic drug panomifene.

Entities:  

Year:  2004        PMID: 15012068     DOI: 10.1021/ol036440n

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  1 in total

1.  Highly stereocontrolled synthesis of trans-enediynes via carbocupration of fluoroalkylated diynes.

Authors:  Tsutomu Konno; Misato Kishi; Takashi Ishihara
Journal:  Beilstein J Org Chem       Date:  2012-12-19       Impact factor: 2.883

  1 in total

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