Literature DB >> 25000554

A phosphine-mediated stereocontrolled synthesis of Z-enediynes by a vicinal dialkynylation of ethynylphosphonium salts.

Kyle D Reichl1, Alexander T Radosevich.   

Abstract

Z-Enediynes are prepared by a vicinal dialkynylation of triaryl(arylethynyl)phosphonium cations. The method, which proceeds under mild transition metal-free conditions, can be conducted on multigram scale as a one-pot, phosphine-mediated synthetic cycle giving enediyne products with excellent control of configuration.

Entities:  

Year:  2014        PMID: 25000554     DOI: 10.1039/c4cc03415e

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  3 in total

1.  Heterobiaryl synthesis by contractive C-C coupling via P(V) intermediates.

Authors:  Michael C Hilton; Xuan Zhang; Benjamin T Boyle; Juan V Alegre-Requena; Robert S Paton; Andrew McNally
Journal:  Science       Date:  2018-11-16       Impact factor: 47.728

2.  Synthesis of acyl(chloro)phosphines enabled by phosphinidene transfer.

Authors:  Kevin M Szkop; Michael B Geeson; Douglas W Stephan; Christopher C Cummins
Journal:  Chem Sci       Date:  2019-02-07       Impact factor: 9.825

Review 3.  Cationic Organophosphorus Chromophores: A Diamond in the Rough among Ionic Dyes.

Authors:  Andrey Belyaev; Pi-Tai Chou; Igor O Koshevoy
Journal:  Chemistry       Date:  2020-10-30       Impact factor: 5.020

  3 in total

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