Literature DB >> 21446697

Radical alkylphosphanylation of olefins with stannylated or silylated phosphanes and alkyl iodides.

Marie-Céline Lamas1, Armido Studer.   

Abstract

Intermolecular conjugate radical addition reactions of secondary and tertiary alkyl radicals derived from the corresponding alkyl iodides to activated olefins such as α,β-unsaturated esters, amides, imides, nitriles, and sulfones are described. The adduct radicals are trapped by either diphenyl(trimethylstannyl)phosphane or the commercially available diphenyl(trimethylsilyl)phosphane as chain transfer reagents to give the corresponding phosphanylated products in moderate to good yields. The overall process comprises a C-C followed by a C-P bond formation.

Entities:  

Year:  2011        PMID: 21446697     DOI: 10.1021/ol200483p

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


  2 in total

1.  An Electroreductive Approach to Radical Silylation via the Activation of Strong Si-Cl Bond.

Authors:  Lingxiang Lu; Juno C Siu; Yihuan Lai; Song Lin
Journal:  J Am Chem Soc       Date:  2020-12-08       Impact factor: 15.419

2.  Homolytic substitution at phosphorus for C-P bond formation in organic synthesis.

Authors:  Hideki Yorimitsu
Journal:  Beilstein J Org Chem       Date:  2013-06-28       Impact factor: 2.883

  2 in total

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