Literature DB >> 19728703

A general procedure for the preparation of beta-ketophosphonates.

Kevin M Maloney1, John Y L Chung.   

Abstract

A mild, high-yielding procedure for the preparation of beta-ketophosphonates is described. The condensation is general with respect to the ester and phosphonate, and the products are obtained in high yields within minutes at 0 degrees C. The reaction procedure is operationally simple and amenable to large-scale preparations.

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Year:  2009        PMID： 19728703     DOI： 10.1021/jo901552k

Source DB:  PubMed          Journal:  J Org Chem        ISSN： 0022-3263            Impact factor:   4.354


  4 in total

1.  β-Keto and β-hydroxyphosphonate analogs of biotin-5'-AMP are inhibitors of holocarboxylase synthetase.

Authors:  Wantanee Sittiwong; Elizabeth L Cordonier; Janos Zempleni; Patrick H Dussault
Journal:  Bioorg Med Chem Lett       Date:  2014-11-07       Impact factor: 2.823

2.  X-ray Characterization and Structure-Based Optimization of Striatal-Enriched Protein Tyrosine Phosphatase Inhibitors.

Authors:  Michael R Witten; Lisa Wissler; Melanie Snow; Stefan Geschwindner; Jon A Read; Nicholas J Brandon; Angus C Nairn; Paul J Lombroso; Helena Käck; Jonathan A Ellman
Journal:  J Med Chem       Date:  2017-11-08       Impact factor: 7.446

Review 3.  Recent trends in the direct oxyphosphorylation of C-C multiple bonds.

Authors:  Alireza Bakhtiary; Mohammad Reza Poor Heravi; Akbar Hassanpour; Issa Amini; Esmail Vessally
Journal:  RSC Adv       Date:  2020-12-23       Impact factor: 3.361

4.  Bioinspired total synthesis of katsumadain A by organocatalytic enantioselective 1,4-conjugate addition.

Authors:  Yongguang Wang; Ruiyang Bao; Shengdian Huang; Yefeng Tang
Journal:  Beilstein J Org Chem       Date:  2013-08-06       Impact factor: 2.883
  4 in total

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