Pure Appl. Chem., ASAP article
http://dx.doi.org/10.1351/PAC-CON-11-09-05
Published online 2012-02-03
Accessing chemical diversity by stereoselective gold-catalyzed manipulation of allylic and propargylic alcohols
Abstract:
The combined use of asymmetric Au(I) catalysis with allylic as well as propargylic alcohols proved to be a competent synthetic tool, toward the realization of complex molecular organic architectures in a stereochemically defined manner. In particular, allylic alcohols have been utilized as alkylating agents in the synthesis of tetrahydrocarbazoles/carbolines and morpholines by means of new C–C and C–X bond-forming processes. Analogously, the direct activation of indole-propargylic alcohols with cationic Au complexes opened a direct access to tetracyclic fused indolines in a highly stereoselective manner.
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