A crystalline, internally-coordinated chloroborane for asymmetric hydroboration
Author:
Funder
National Science Foundation
National Institutes of Health
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference45 articles.
1. Hydroboration as a convenient procedure for the asymmetric synthesis of alcohols of high optical purity. Journal of the American chemical society;Brown;American Chem. Soc.,1961
2. Hydroboration. 61. Diisopropylamine of high optical purity. Improved preparation and asymmetric hydroboration of representative cis-disubstituted alkenes;Brown;J. Org. Chem.,1982
3. Monoisopinocampheylborane—a new chiral hydroborating agent for relatively hindered (trisubstituted) olefins;Brown;J. Am. Chem. Soc.,1977
4. Hydroboration. 62. Monoisopinocampheylborane, an excellent chiral hydroborating agent for trans-disubstituted and trisubstituted alkenes. Evidence for a strong steric dependence in such asymmetric hydroborations;Brown;J. Org. Chem.,1982
5. Simple synthesis of monoisopinocampheylborane of high optical purity;Brown;J. Org. Chem.,1978
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