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Articles

Total synthesis of (+/ − )-4-demethylenglerin A

, , , , , & show all
Pages 629-639 | Received 14 Apr 2014, Accepted 21 Apr 2014, Published online: 09 Jun 2014
 

Abstract

Racemic 4-demethylenglerin A (1′), a simplified analog of the guaiane-type sesquiterpene englerin A (1), has been synthesized. The cyclic hydrocarbon core structure was built through modified Metz approach using epoxynitrile cyclization and direct Aldol reaction to prepare the precursor of RCM. The primary cytotoxicity test summarized that C4 methyl has marked impacts on the bioactivity.

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