Literature DB >> 23327616

Total synthesis of chaetoquadrins A-C.

U Bin Kim1, Daniel P Furkert, Margaret A Brimble.   

Abstract

The first total synthesis of the monoamine oxidase inhibitors chaetoquadrins A-C has been accomplished. Key steps in the synthesis include an aromatic Claisen rearrangement, asymmetric boron aldol reaction and acid-mediated spiroketalization. Comparison of spectral data for the synthetic spiroketals confirmed the proposed structure for these natural products.

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Year:  2013        PMID: 23327616     DOI: 10.1021/ol303482k

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


  1 in total

1.  Application of Mannich bases to the synthesis of hydroxymethylated isoflavonoids as potential antineoplastic agents.

Authors:  Mykhaylo S Frasinyuk; Galyna P Mrug; Svitlana P Bondarenko; Vitaliy M Sviripa; Wen Zhang; Xianfeng Cai; Michael V Fiandalo; James L Mohler; Chunming Liu; David S Watt
Journal:  Org Biomol Chem       Date:  2015-09-29       Impact factor: 3.876

  1 in total

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