Stereoselective Hydrogenation and Ozonolysis of Iridoids. Conversion into Carbocyclic Nucleoside Analogues
Author:
Affiliation:
1. Department of Organic Chemistry, The Technical University of Denmark, Building 201, DK-2800, Lyngby, Denmark, and Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/np990288%2B
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1. Conversion of asperuloside to optically active prostaglandin intermediates
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