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Updated: Dec 29, 2025

Preparation of a Corannulene-functionalized Hexahelicene by CopperI-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
Enantioselective Total Synthesis of (+)-Corymine and (-)-Deformylcorymine
Benxiang Zhang1, Xiaoqing Wang1, Chaozhong Li1,2
1Key Laboratory of Organofluorine Chemistry, Center for Excellence in Molecular Synthesis , Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences , 345 Lingling Road , Shanghai 200032 , P.R. China.
Abstract:
We report herein the first enantioselective total synthesis of akuammiline alkaloids (+)-corymine and (-)-deformylcorymine. Starting from commercially available N-nosyltryptamine, the target molecules are both achieved in 11 steps. Key elements of the design include (a) a copper-catalyzed enantioselective addition of dimethyl malonate to a 3-bromooxindole to secure the C7 all-carbon quaternary stereocenter, (b) a one-step construction of cyclohexyl and pyrrolidinyl rings via intramolecular nucleophilic C- and N-addition, and (c) a nickel-promoted 7-endo cyclization of alkenyl bromide to furnish the azepanyl ring. The strategy is further extended to the synthesis of another three members of the akuammiline family, namely, (-)-10-demethoxyvincorine, (-)-2(S)-cathafoline, and (-)-3-epi-dihydrocorymine 17-acetate.
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