4.7 Article

Synthetic studies on vincorine: access to the 3a,8a-dialkyl-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indole skeleton

Journal

CHEMICAL COMMUNICATIONS
Volume -, Issue 28, Pages 4275-4277

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/b907210a

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Funding

  1. Ministry of Education, Culture, Sports, Science and Technology of Japan

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Synthetic studies on vincorine are described; the conversion of 3-aminoethyl-3-alkyloxindoles to 3a,8a-dialkyl-1,2,3,3a,8,8a-hexahydropyrrolo[2,3-b]indoles has been achieved through an addition-cyclization sequence, and a fully functionalized key intermediate was constructed with this method.

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