Literature DB >> 23321719

Efficient synthesis of silylated 2,2-difluorostyrene derivatives through Suzuki-Miyaura cross-coupling of 2,2-difluoro-1-iodo-1-silylethenes.

Marc-Olivier Turcotte-Savard1, Jean-François Paquin.   

Abstract

We report a new synthetic sequence for the preparation of silylated 2,2-difluorostyrene derivatives. This new route has numerous advantages over the previous one including enhanced scope, higher yields, ease of purification, and significant reduction of the amount of desilylated side-products. An unexpected transformation of a silylated 2,2-difluorostyrene derivative is also presented.

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Year:  2013        PMID: 23321719     DOI: 10.1039/c2ob27221k

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  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

  1 in total

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