4.5 Article

Cyclocondensation Reactions between 2-Acyl-3-indoleacetic Acid Derivatives and Phenylglycinol: Enantioselective Synthesis of 1-Substituted Tetrahydro-ß-carboline Alkaloids

期刊

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2012, 期 9, 页码 1835-1842

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201101718

关键词

Asymmetric synthesis; Total synthesis; Alkaloids; Nitrogen heterocycles; Lactams

资金

  1. Spanish Ministry of Science and Innovation (MICINN) [CTQ2009-07021/BQU]
  2. Agencia de Gestio d'Ajuts Universitaris i de Recerca (AGAUR), Generalitat de Catalunya [2009-SGR-1111]

向作者/读者索取更多资源

Cyclocondensation reactions between a variety of 2-acyl-3-indoleacetic acid derivatives and (R)-phenylglycinol were studied. Successful results were obtained from N-alkyl keto acid derivatives. The resulting tetracyclic lactams provide straightforward access to enantiopure 1-substituted tetrahydro-beta-carboline alkaloids.

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