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Concise Enantiospecific Total Synthesis of Tubingensin A

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Journal J Am Chem Soc
Specialty Chemistry
Date 2014 Feb 15
PMID 24524351
Citations 26
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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.

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