Author:
Czarnocki Zbigniew,Maclean David B.,Szarek Walter A.
Abstract
The utility of the Pictet–Spengler condensation of (R)-(+)-glyceraldehyde with dopamine hydrochloride in the enantioselective synthesis of isoquinoline alkaloids is demonstrated by the preparation of (S)-(−)-carnegine, (R)-(−)-calycotomine, and (S)-(+)-laudanosine.
Publisher
Canadian Science Publishing
Subject
Organic Chemistry,General Chemistry,Catalysis
Cited by
54 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Design and synthesis of novel phenyl -1, 4-beta-carboline-hybrid molecules as potential anticancer agents;European Journal of Medicinal Chemistry;2017-03
2. Synthesis of 6,7-Dimethoxy-1,3,4,8b-Tetrahydroazirino [2,1-a]Isoquinoline-N-Borane and bis-(6,7-Dimethoxy-1,2,3,4-Tetrahydroisoquinoline)-1,1′-Ene;Chemistry of Natural Compounds;2014-10-29
3. Pictet-Spengler Reaction Revisited: Engineering of Tetherd Biheterocycles into Annulated Polyheterocycles;Current Organic Synthesis;2012-05-01
4. Synthesis of Calycotomine and N-Methylcalycotomine Using a Petasis Reaction — Pomeranz-Fritsch-Bobbitt Cyclization Sequence;HETEROCYCLES;2012
5. Asymmetric Organocatalytic Cyclization and Cycloaddition Reactions;Chemical Reviews;2011-05-26