Chiral Ligands Derived from Monoterpenes: Application in the Synthesis of Optically Pure Secondary Alcohols via Asymmetric Catalysis

被引:55
|
作者
Ibn El Alami, Mohammed Samir [1 ]
Amin El Amrani, Mohamed [1 ]
Agbossou-Niedercorn, Francine [2 ]
Suisse, Isabelle [2 ]
Mortreux, Andre [2 ]
机构
[1] Univ Abdelmalek Essaadi, Lab Chim Organ Appl, Fac Sci, Tetouan, Morocco
[2] Univ Lille Nord France, UMR CNRS 8181, UCCS, ENSCL, F-59652 Villeneuve Dascq, France
关键词
alcohols; asymmetric catalysis; chiral ligands; natural product synthesis; terpenes; HIGHLY ENANTIOSELECTIVE ADDITION; TRANSFER HYDROGENATION; BORANE REDUCTION; PROCHIRAL KETONES; AMINO-ALCOHOLS; N-OXIDES; STEREOSELECTIVE-SYNTHESIS; TERPENE AUXILIARIES; CARBONYL-COMPOUNDS; ALPHA-PINENE;
D O I
10.1002/chem.201404303
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The preparation of optically pure secondary alcohols in the presence of catalysts based on chiral ligands derived from monoterpenes, such as pinenes, limonenes and carenes, is reviewed. A wide variety of these ligands has been synthesized and used in several catalytic reactions, including hydrogen transfer, C-C bond formation via addition of organozinc compounds to aldehydes, hydrosilylation, and oxazaborolidine reduction, leading to high activities and enantioselectivities.
引用
收藏
页码:1398 / 1413
页数:16
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