Asymmetric Transformation of Either Enantiomer of Narwedine via Total Spontaneous Resolution Process, a Concise Solution to the Synthesis of (-)-Galanthamine

Asymmetric Transformation of Either Enantiomer of Narwedine via Total Spontaneous Resolution Process, a Concise Solution to the Synthesis of (-)-Galanthamine

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Bibliographic Details
Published in:Journal of organic chemistry Vol. 59; no. 18; pp. 5463 - 5465
Main Authors: Shieh, Wen-Chung, Carlson, John A
Format: Journal Article
Language:English
Published: Washington, DC American Chemical Society 01-09-1994
Subjects:
Chemistry
Exact sciences and technology
Heterocyclic compounds
Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms
Organic chemistry
Preparations and properties
Catalytic reaction
Enzyme
Enzyme inhibitor
Esterases
Tetracyclic compound
Acetylcholinesterase
Diastereoselectivity
Carboxylic ester hydrolases
Chemical reduction
Alkaloid
Optical resolution
Hydrolases
Aromatic compound
Enantiomer(-)
Oxygen nitrogen heterocycle
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Description
Bibliography:ark:/67375/TPS-5XD7GWL5-D
istex:7A8C1E61020DCA9F33CBD291BF6CDE3D8CB4C47A
ISSN:0022-3263
1520-6904
DOI:10.1021/jo00097a060