Literature DB >> 11796052

Rapid synthesis of the 7-deoxy zaragozic acid core.

Michael A Calter1, Cheng Zhu, Rene J Lachicotte.   

Abstract

[reaction: see text] We have developed an efficient synthesis of the 7-deoxy zaragozic acid core. The synthesis begins with a Feist-Bénary reaction that assembles all three carbons of the polycarboxylic acid portion of the core. This reaction is followed by highly diastereoselective aldol and dihydroxylation reactions that set the remaining stereocenters of the core. The synthesis finishes with lactol oxidation and lactone alcoholysis/ketal formation reactions to construct the bicyclic ring system of the core.

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Year:  2002        PMID: 11796052     DOI: 10.1021/ol0169980

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


  3 in total

1.  Catalytic, asymmetric, interrupted Feist-Bénary reactions of α-tosyloxyacetophenones.

Authors:  Michael A Calter; Alexander Korotkov
Journal:  Org Lett       Date:  2011-11-04       Impact factor: 6.005

2.  A facile metal-free one-flask synthesis of multi-substituted furans via a BF3·Et2O mediated formal [4 + 1] reaction of 3-chloro-3-phenyldiazirines and α,β-alkenyl ketones.

Authors:  Zixin Zhang; Aimin Huang; Lin Ma; Jian-Hua Xu; Min Zhang
Journal:  RSC Adv       Date:  2022-05-18       Impact factor: 4.036

3.  Structure-Based Design, Synthesis and Biological Evaluation of Bis-Tetrahydropyran Furan Acetogenin Mimics Targeting the Trypanosomatid F1 Component of ATP Synthase.

Authors:  Marija K Zacharova; Lindsay B Tulloch; Eoin R Gould; Andrew L Fraser; Elizabeth F King; Stefanie K Menzies; Terry K Smith; Gordon J Florence
Journal:  European J Org Chem       Date:  2019-05-29
  3 in total

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