Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/13010
Title: The enantioselective formal synthesis of rhynchophylline and isorhynchophylline
Authors: Zhang, H
Ma, X
Kang, H
Hong, L
Wang, R
Keywords: cascade reactions
natural products
organocatalysis
total synthesis
Issue Date: 2013
Publisher: Wiley-V C H Verlag Gmbh
Source: Chemistry - an Asian journal, 2013, v. 8, no. 3, p. 542-545 How to cite?
Journal: Chemistry - An Asian Journal 
Abstract: Formal attire: An enantioselective formal total synthesis of the alkaloids isorhynchophylline and rhynchophylline is described. The key steps include an organocatalyzed asymmetric Michael addition reaction and an efficient diastereoselective intramolecular iminium ion spirocyclization/lactamization cascade sequence.
URI: http://hdl.handle.net/10397/13010
ISSN: 1861-4728
DOI: 10.1002/asia.201201046
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