4.8 Article

A new, iterative strategy for the synthesis of unsymmetrical polyynes: Application to the total synthesis of 15,16-dihydrominquartynoic acid

Journal

ORGANIC LETTERS
Volume 6, Issue 20, Pages 3601-3604

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol0484963

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A new iterative strategy for the synthesis of unsymmetrically substituted polyynes has been developed. The starting bromoalkyne is homologated by one acetylene unit through palladium-catalyzed cross-coupling with a TIPS-protected terminal acetylene and a subsequent in situ one-pot AgF-mediated desilylative bromination. The utility of this new synthetic method is demonstrated by its application to the total synthesis of (S)-(E)-15,16-dihydrominquartynoic acid.

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