Ontology highlight
ABSTRACT:
SUBMITTER: Mandel AL
PROVIDER: S-EPMC2736336 | biostudies-other | 2009 Aug
REPOSITORIES: biostudies-other
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]