4.5 Article

Total Syntheses of Eudistomins Y1-Y7 by an Efficient One-Pot Process of Tandem Benzylic Oxidation and Aromatization of 1-Benzyl-3,4-dihydro-β-Carbolines

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2013, 期 16, 页码 3271-3277

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201300080

关键词

Natural products; Alkaloids; Total synthesis; Nitrogen heterocycles; Aromatization

资金

  1. National Natural Science Foundation of China (NSFC) [20972048]
  2. Shanghai Educational Development Foundation [03SG27]
  3. Ministry of Education and Training, Vietnam

向作者/读者索取更多资源

The first total synthesis of eudistomin Y-7 (7) and total syntheses of eudistomins Y-1-Y-6 (1-6) are described. An efficient room-temperature conversion of 1-benzyl-3,4-dihydro-beta-carbolines (11) into 1-benzoyl-beta-carbolines (14) by a one-pot process of tandem benzylic oxidation and aromatization as the key step of these total syntheses was also studied in detail.

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