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Concise enantiospecific total synthesis of tubingensin A.

ABSTRACT: We report the enantiospecific total synthesis of (+)-tubingensin A. Our synthesis features an aryne cyclization to efficiently introduce the vicinal quaternary stereocenters of the natural product and proceeds in only nine steps (longest linear sequence) from known compounds.

SUBMITTER: Goetz AE

PROVIDER: S-EPMC3985696 | biostudies-literature | 2014 Feb

REPOSITORIES: biostudies-literature

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Concise enantiospecific total synthesis of tubingensin A.

Goetz Adam E AE Silberstein Amanda L AL Corsello Michael A MA Garg Neil K NK

Journal of the American Chemical Society 20140218 8

We report the enantiospecific total synthesis of (+)-tubingensin A. Our synthesis features an aryne cyclization to efficiently introduce the vicinal quaternary stereocenters of the natural product and proceeds in only nine steps (longest linear sequence) from known compounds. ...[more]

PMID: 24524351

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