Literature DB >> 20491504

Diversity-oriented synthesis of disubstituted alkenes using masked silanols.

Hannah F Sore1, David T Blackwell, Simon J F Macdonald, David R Spring.   

Abstract

The regio- and stereoselective synthesis and subsequent Hiyama cross coupling of pentafluorophenyldimethylvinylsilanes has been developed, thus providing a convenient and robust method for the diversity-oriented synthesis of (E)-, (Z)- and alpha-disubstituted alkenes from terminal alkynes. Pentafluorophenyldimethylvinylsilanes undergo cross-coupling reactions with excellent selectivity and in good yields, offering an attractive alternative to existing masked silanols.

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Year:  2010        PMID: 20491504     DOI: 10.1021/ol100895d

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


  2 in total

1.  (Z)-(2-bromovinyl)-MIDA boronate: a readily accessible and highly versatile building block for small molecule synthesis.

Authors:  Eric M Woerly; Justin R Struble; Nagarjuna Palyam; Sean P O'Hara; Martin D Burke
Journal:  Tetrahedron       Date:  2011-06-17       Impact factor: 2.457

2.  Regioselective allene hydroarylation via one-pot allene hydrosilylation/Pd-catalyzed cross-coupling.

Authors:  Zachary D Miller; John Montgomery
Journal:  Org Lett       Date:  2014-10-02       Impact factor: 6.005

  2 in total

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