Application of Chiral Lanthanide Shift Reagents for Assignment of Absolute Configuration of Alcohols
Author:
Affiliation:
1. Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol048061f
Reference24 articles.
1. Toward the Creation of NMR Databases in Chiral Solvents: Bidentate Chiral NMR Solvents for Assignment of the Absolute Configuration of Acyclic Secondary Alcohols
2. Application of chiral bidentate NMR solvents for assignment of the absolute configuration of alcohols: scope and limitation
3. Glisoprenins, new inhibitors of acyl-CoA: Cholesterol acyltransferase produced by Gliocladium sp. FO-1513. I. Production, isolation and physico-chemical and biological properties.
4. Glisoprenins, new inhibitors of acyl-CoA: Cholesterol acyltransferase produced by Gliocladium sp. FO-1513. II. Structure elucidation of glisoprenins A and B.
5. Use of a Chiral Praseodymium Shift Reagent in Predicting the Complete Stereostructure of Glisoprenin A
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