Literature DB >> 16292853

Enol tosylates as viable partners in Pd-catalyzed cross-coupling reactions.

Dietrich Steinhuebel1, Jenny M Baxter, Michael Palucki, Ian W Davies.   

Abstract

[reaction: see text] Herein we demonstrate functionalized enol tosylates to be robust substrates that undergo Suzuki-Miyaura, Sonogashira, and Stille cross-coupling reactions to provide stereodefined trisubstituted unsaturated esters.

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Year:  2005        PMID： 16292853     DOI： 10.1021/jo051590s

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


  3 in total

1.  Cross-Coupling Reactions of Alkenylsilanols with Fluoroalkylsulfonates: Development and Optimization of a Mild and Stereospecific Coupling Process.

Authors:  Scott E Denmark; Christopher S Regens
Journal:  Tetrahedron Lett       Date:  2011-04-27       Impact factor: 2.415

2.  STILLE CROSS-COUPLING REACTIONS OF ARYL MESYLATES AND TOSYLATES USING A BIARYLPHOSPHINE BASED CATALYST SYSTEM.

Authors:  John R Naber; Brett P Fors; Xiaoxing Wu; Jonathon Gunn; Stephen L Buchwald
Journal:  Heterocycles       Date:  2010-02-26       Impact factor: 0.831

3.  Consecutive cross-coupling reactions of 2,2-difluoro-1-iodoethenyl tosylate with boronic acids: efficient synthesis of 1,1-diaryl-2,2-difluoroethenes.

Authors:  Ju Hee Kim; Su Jeong Choi; In Howa Jeong
Journal:  Beilstein J Org Chem       Date:  2013-11-14       Impact factor: 2.883
  3 in total

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