Oxidative Homocoupling of Chiral 3-Arylpropanoic Acid Derivatives. Application to Asymmetric Synthesis of Lignans
Author:
Affiliation:
1. Department of Biotechnology, Faculty of Engineering, Tottori University, Tottori 680-0945, Japan
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo991317o
Reference32 articles.
1. (a) Ayres, D. C.; Loike, J. D.Lignans; Cambridge University Press: Cambridge, 1990.
2. Asymmetric synthesis of lignans
3. General conjugate-addition method for the synthesis of enantiomerically pure lignans. Total synthesis of (-)- and (+)-burseran, (-)-dehydroxycubebin, (-)-trichostin, (-)-cubebin, (-)-5''-methoxyhinokinin, and (-)-hinokinin
4. Conjugate addition to chiral γ-heterosubstituted δ-lactones as pivotal synthons from L-glutamic acid. Synthesis of an optically active lignan lactone; (−)-hinokinin
5. An efficient enantioselective total synthesis of antitumor lignans: synthesis of enantiomerically pure 4-hydroxyalkanenitriles via an enzymic reaction
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