A stereoselective synthesis of (+)-physoperuvine using a tandem aza-Claisen rearrangement and ring closing metathesis reaction
A stereoselective synthesis of (+)-physoperuvine, a tropane alkaloid from Physalis peruviana Linne has been developed using a one-pot tandem aza-Claisen rearrangement and ring closing metathesis reaction to form the key amino-substituted cycloheptene ring
Zaed, Ahmed M.,Swift, Michael D.,Sutherland, Andrew
supporting information; experimental part
p. 2678 - 2680
(2009/09/08)
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