Literature DB >> 26393932

Total synthesis of (-)-depyranoversicolamide B.

Wen-Fang Qin1, T Xiao1, D Zhang2, Lin-Feng Deng2, Y Wang2, Y Qin2.   

Abstract

Starting from easily prepared (R)-C3-isoprenylated pyrroloindoline, the C3-isoprenylated indolyl diketopiperazine is prepared by an efficient reductive opening of the pyrrolo ring, and undergoes biomimetic Diels-Alder reaction to generate an anti-adduct as a sole stereoisomer. Oxidation of the indoline moiety to oxindole completes the synthesis of (-)-depyranoversicolamide B.

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Year:  2015        PMID: 26393932     DOI: 10.1039/c5cc05877e

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


  2 in total

1.  Brevianamides and Mycophenolic Acid Derivatives from the Deep-Sea-Derived Fungus Penicillium brevicompactum DFFSCS025.

Authors:  Xinya Xu; Xiaoyong Zhang; Xuhua Nong; Jie Wang; Shuhua Qi
Journal:  Mar Drugs       Date:  2017-02-17       Impact factor: 5.118

2.  Unified total synthesis of the brevianamide alkaloids enabled by chemical investigations into their biosynthesis.

Authors:  Robert C Godfrey; Helen E Jones; Nicholas J Green; Andrew L Lawrence
Journal:  Chem Sci       Date:  2021-12-29       Impact factor: 9.825

  2 in total

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