Literature DB >> 11558613

Improved preparation of sulfur substituted 3-vinylpyrrole and its application to the syntheses of chuangxinmycin derivatives.

T Yoshida1, A Ito, K Ibusuki, M Murase, E Kotani.   

Abstract

Sulfur substituted 3-vinylpyrrole 10 was prepared from 3-thio-acetylpyrrole 9 by alkylation with alkyl halide in the presence of propylene oxide. Functionalized 4-alkylthioindoles were made by Diels-Alder reaction of the 3-vinylpyrrole 10 with dienophiles. Chuangxinmycin analogues were synthesized by using some of the functionalized 4-alkylthioindoles as key intermediates.

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Year:  2001        PMID: 11558613     DOI: 10.1248/cpb.49.1198

Source DB:  PubMed          Journal:  Chem Pharm Bull (Tokyo)        ISSN: 0009-2363            Impact factor:   1.645


  1 in total

1.  Biosynthesis of antibiotic chuangxinmycin from Actinoplanes tsinanensis.

Authors:  Yuanyuan Shi; Zhibo Jiang; Xingxing Li; Lijie Zuo; Xuan Lei; Liyan Yu; Linzhuan Wu; Jiandong Jiang; Bin Hong
Journal:  Acta Pharm Sin B       Date:  2017-08-12       Impact factor: 11.413

  1 in total

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