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A versatile route to the tulearin class of macrolactones: synthesis of a stereoisomer of tulearin A.


ABSTRACT: A versatile synthetic approach to the tulearin class of macrolactones has been developed and deployed to make a stereoisomer of tulearin A. The knowledge gained about structure and synthesis will expedite the assignment of the stereostructure of this new anticancer agent.

SUBMITTER: Mandel AL 

PROVIDER: S-EPMC2736336 | biostudies-other | 2009 Aug

REPOSITORIES: biostudies-other

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A versatile route to the tulearin class of macrolactones: synthesis of a stereoisomer of tulearin A.

Mandel Alexander L AL   Bellosta Véronique V   Curran Dennis P DP   Cossy Janine J  

Organic letters 20090801 15


A versatile synthetic approach to the tulearin class of macrolactones has been developed and deployed to make a stereoisomer of tulearin A. The knowledge gained about structure and synthesis will expedite the assignment of the stereostructure of this new anticancer agent. ...[more]

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