Highly Diastereoselective Synthesis of the 1,1‘-Binaphthol Unit on a Bile Acid Template
Author:
Affiliation:
1. Department of Organic Chemistry, Indian Institute of Science, Bangalore 560 012, India
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo000703z
Reference45 articles.
1. 1,1‘-Binaphthyl Dimers, Oligomers, and Polymers: Molecular Recognition, Asymmetric Catalysis, and New Materials
2. Induction of axial dissymmetry into the 1,1′-binaphthyl bond via an intramolecular ullmann coupling reaction
3. 1,1'-Binaphthalene-2,2'-diol as a Chiral Auxiliary. Diastereoselective Alkylation of Binaphthyl Esters, Complex-Induced Proximity Effects in Enolate Formation, and One-Step Synthesis of an Optically Active .beta.-Substituted Ketone
4. Virtually complete enantioface differentiation in carbonyl group reduction by a complex aluminum hydride reagent
5. Highly enantioselective reduction of alkynyl ketones by a binaphthol-modified aluminum hydride reagent. Asymmetric synthesis of some insect pheromones
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