Literature DB >> 15330629

First total synthesis of the antitumor compound (-)-kazusamycin A and absolute structure determination.

Noriyoshi Arai1, Noriko Chikaraishi, Satoshi Omura, Isao Kuwajima.   

Abstract

The first total synthesis of kazusamycin A, a potent antitumor compound from an actinomycete, has been achieved, and its absolute structure was determined. Paterson's stereoselective aldol reaction was successfully applied to construct the contiguous chiral centers by using an originally designed optically active 2-acyl-1,3-propanediol derivative. Copyright 2004 American Chemical Society

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Year:  2004        PMID: 15330629     DOI: 10.1021/ol049219z

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


  2 in total

1.  Regioselective Reductive Cross-Coupling Reactions of Unsymmetrical Alkynes.

Authors:  Holly A Reichard; Martin McLaughlin; Ming Z Chen; Glenn C Micalizio
Journal:  European J Org Chem       Date:  2010-01

2.  Trapping Hemiacetals with Phosphono Substituted Palladium π-Allyl Complexes for the Synthesis of Substituted Cyclic Ethers.

Authors:  Nongnuch Sutivisedsak; Surendra Dawadi; Christopher D Spilling
Journal:  Tetrahedron Lett       Date:  2015-06-03       Impact factor: 2.415

  2 in total

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