Literature DB >> 15136847

Synthetic approach to kendomycin: preparation of the C-glycosidic core.

Tetsuya Sengoku1, Hirokazu Arimoto, Daisuke Uemura.   

Abstract

Synthesis of the C13-C19 C-glycoside portion of kendomycin was achieved via oxidative pyran cyclization and Claisen rearrangement to construct the fully functionalized aromatic ring.

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Year:  2004        PMID: 15136847     DOI: 10.1039/b402391a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

Review 1.  Strategies for construction of the all-carbon macrocyclic skeleton of the ansamycin antibiotic-kendomycin.

Authors:  Shu Xu; Hirokazu Arimoto
Journal:  J Antibiot (Tokyo)       Date:  2016-02-10       Impact factor: 2.649

2.  Total synthesis of kendomycin: a macro-C-glycosidation approach.

Authors:  Yu Yuan; Hongbin Men; Chulbom Lee
Journal:  J Am Chem Soc       Date:  2004-11-17       Impact factor: 15.419

  2 in total

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