Literature DB >> 11681952

Stille cross-coupling reaction of an alpha-stannyl enamide.

S Minière1, J C Cintrat.   

Abstract

The Stille cross-coupling reaction of an N-tosyl alpha-stannyl enamine is clearly exemplified for the first time with a wide range of halogeno derivatives. This gives access to functionalized alpha-substituted enamines in fair yields.

Entities:  

Year:  2001        PMID： 11681952     DOI： 10.1021/jo015824t

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


  3 in total

Review 1.  Ynamides: a modern functional group for the new millennium.

Authors:  Kyle A DeKorver; Hongyan Li; Andrew G Lohse; Ryuji Hayashi; Zhenjie Lu; Yu Zhang; Richard P Hsung
Journal:  Chem Rev       Date:  2010-09-08       Impact factor: 60.622

2.  Scope and limitation of propylene carbonate as a sustainable solvent in the Suzuki-Miyaura reaction.

Authors:  Andrea Czompa; Balázs László Pásztor; Jennifer Alizadeh Sahar; Zoltán Mucsi; Dóra Bogdán; Krisztina Ludányi; Zoltán Varga; István M Mándity
Journal:  RSC Adv       Date:  2019-11-20       Impact factor: 4.036

3.  Copper-mediated N-alkynylation of carbamates, ureas, and sulfonamides. A general method for the synthesis of ynamides.

Authors:  Joshua R Dunetz; Rick L Danheiser
Journal:  Org Lett       Date:  2003-10-16       Impact factor: 6.005
  3 in total

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