Literature DB >> 11029205

Orthosilicate-mediated esterification of monosubstituted phosphinic acids

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Abstract

Monosubstituted phosphinic acids are esterified with orthosilicates in excellent yields. Phosphinylidene-containing acids react selectively under these conditions, while disubstituted phosphinic acids and phosphonic acids remain unchanged. One-pot procedures are also described for the preparation of phosphinate esters from an alcohol. This novel method provides a convenient and general alternative to more commonly employed conditions such as diazomethane or carbodiimide.

Entities:  

Year:  2000        PMID: 11029205     DOI: 10.1021/ol006434g

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


  4 in total

1.  Alkylation of H-phosphinate esters under basic conditions.

Authors:  Isabelle Abrunhosa-Thomas; Claire E Sellers; Jean-Luc Montchamp
Journal:  J Org Chem       Date:  2007-03-13       Impact factor: 4.354

2.  Green, Palladium-Catalyzed Synthesis of Benzylic H-phosphinates from Hypophosphorous Acid and Benzylic Alcohols.

Authors:  Laëtitia Coudray; Jean-Luc Montchamp
Journal:  European J Org Chem       Date:  2008-08-01

3.  Temporary Protection of H-Phosphinic Acids as a Synthetic Strategy.

Authors:  Laëtitia Coudray; Jean-Luc Montchamp
Journal:  European J Org Chem       Date:  2009-09

Review 4.  Let's Make White Phosphorus Obsolete.

Authors:  Michael B Geeson; Christopher C Cummins
Journal:  ACS Cent Sci       Date:  2020-05-18       Impact factor: 14.553

  4 in total

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