Density functional study on enantioselective reduction of keto oxime ether with borane catalyzed by oxazaborolidine
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Chemistry
Link
http://link.springer.com/content/pdf/10.1007/s11426-006-2008-7.pdf
Reference24 articles.
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2. Soai K, Niwa S. Enantioselective addition of organozine reagents to aldehydes. Chem Rev, 1992, 92: 833–856
3. Blaser H U. The chiral pool as a source of enantioselective catalysts and auxiliaries. Chem Rev, 1992, 92: 935–952
4. Tillyer R D, Baudreau C, Tschaen D, Dolling U H, Reider P J. Asymmetric reduction of keto oxime ethers using oxazaborolidine reagents: The enantioselective synthesis of cyclic amino alcohols. Tetrahedron Lett, 1995, 36: 4337–4340
5. Nevalainen V. Quantum chemical modeling of chiral catalysis: Part 3. On the role of a Lewis basic solvent in the mechanism of catalytic enantioselective reduction of carbonyl compounds by chiral oxazaborolidines. Tetrahedron: Asymmetry, 1991, 2: 827–842
Cited by 2 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. The B–H–B bridging interaction in B-substituted oxazaborolidine–borane complexes: a theoretical study;Structural Chemistry;2012-12-18
2. Density functional theory study on the insertion reaction mechanism of dibromocarbene with formaldehyde;Chinese Science Bulletin;2007-08
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