yuremamine has been researched along with 1-1-cyclopropanedicarboxylate* in 1 studies
1 other study(ies) available for yuremamine and 1-1-cyclopropanedicarboxylate
Article | Year |
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Expedient synthesis of pyrrolo[1,2-a]indoles: preparation of the core of yuremamine.
Pyrrolo[1,2- a]indoles are conveniently prepared from tetrahydro-1,2-oxazines, which in turn are generated through the reaction of nitrones with 1,1-cyclopropanediesters. The synthetic route proves to be highly diastereoselective and provides access to the core of the recently discovered pyrrolo[1,2- a]indole natural product yuremamine. Topics: Dicarboxylic Acids; Indoles; Molecular Structure; Nitrogen Oxides; Oxazines; Plant Extracts; Pyrroles; Stereoisomerism | 2008 |