Literature DB >> 16568994

Radical phosphination of organic halides and alkyl imidazole-1-carbothioates.

Akinori Sato1, Hideki Yorimitsu, Koichiro Oshima.   

Abstract

Taking advantage of a radical-based methodology, mild and chemoselective phosphination reactions of organic halide and alkyl imidazole-1-carbothioates have been developed. The mild reaction conditions allow labile functional groups to survive during the reaction.

Entities:  

Year:  2006        PMID: 16568994     DOI: 10.1021/ja058783h

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  3 in total

1.  Synthesis of monophosphines directly from white phosphorus.

Authors:  Daniel J Scott; Jose Cammarata; Maximilian Schimpf; Robert Wolf
Journal:  Nat Chem       Date:  2021-04-05       Impact factor: 24.427

2.  Photoinduced Bisphosphination of Alkynes with Phosphorus Interelement Compounds and Its Application to Double-Bond Isomerization.

Authors:  Yuki Yamamoto; Ryo Tanaka; Shintaro Kodama; Akihiro Nomoto; Akiya Ogawa
Journal:  Molecules       Date:  2022-02-14       Impact factor: 4.411

3.  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

  3 in total

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