A convenient route for the synthesis of s,s-and R,R-warfarin alcohols
Author:
Publisher
Wiley
Subject
Organic Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/jhet.5570220265/fullpdf
Reference4 articles.
1. S. Preis, B. D. West and K. P. Link, US Patent 3,239,529 (March 8, 1966);
2. Chem Abstr., 64, 17547c (1966).
3. Lithium .beta.-isopinocamphenyl-9-borabicyclo[3.3.1]nonyl hydride. A new reagent for the asymmetric reduction of ketones with remarkable consistency
4. Absolute configurations of the four warfarin alcohols
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2. Synthesis and structure–activity relationships of novel warfarin derivatives;Bioorganic & Medicinal Chemistry;2007-03
3. Total Synthesis and Proof of Stereochemistry of Natural and Unnatural Pinnaic Acids: A Remarkable Long-Range Stereochemical Effect in the Reduction of 17-Oxo Precursors of the Pinnaic Acids This work was supported by the National Institutes of Health (Grant Numbers: CA28824). Postdoctoral Fellowship support is gratefully acknowledged by M.W.C. (U.S. Army BCRP, DAMD17-98-1-8154). We thank Dr. George Sukenick of the MSKCC NMR Core Facility for NMR and mass spectral analyses. We would like to thank professor Nakanishi for his supportive interest in the project.;Angewandte Chemie International Edition;2001-12-03
4. Total Synthesis and Proof of Stereochemistry of Natural and Unnatural Pinnaic Acids: A Remarkable Long-Range Stereochemical Effect in the Reduction of 17-Oxo Precursors of the Pinnaic Acids;Angewandte Chemie;2001-12-03
5. Long-distance control in stereoselective reduction of 3-[3-(4?-bromo[1,1?-biphenyl]-4-yl)-3-keto-1-phenylpropyl]-4-hydroxy-2H-1-benzopyran-2-one: Relative configuration of prevailing diastereomer and absolute configuration of its enantiomers;Chirality;1997
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