Directing Effects in the Hydroboration of Steroidal Alkenes
Author:
Affiliation:
1. Department of Chemistry, University of Sussex, Brighton, Sussex BN1 9QJ, UK
Abstract
Publisher
SAGE Publications
Subject
General Chemistry
Link
http://journals.sagepub.com/doi/pdf/10.3184/030823404323000620
Reference37 articles.
1. PelterA., and SmithK. in Comprehensive Organic Synthesis ed. TrostB.M., and FlemingI., Pergamon Press, Oxford, 1991, vol. 8 p. 703.
2. A New Powerful Reducing Agent—Sodium Borohydride in the Presence of Aluminum Chloride and Other Polyvalent Metal Halides1,2
3. Relative rate of exo addition to norbornene and 7,7-dimethylnorbornene. New criterion for distinguishing between cyclic and noncyclic addition processes
4. Hydroboration. II. A Remarkably Fast Addition of Diborane to Olefins—Scope and Stoichiometry of the Reaction
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1. Steroids: partial synthesis in medicinal chemistry;Nat. Prod. Rep.;2006
2. Directing Effects in the Hydroboration of Steroidal Alkenes.;ChemInform;2004-08-31
3. Directing Effects in the Hydroboration of Steroidal Alkenes;ChemInform;2004-08-17
4. An unusual hydroboration of 3-hydroxy-3-methyl-Δ4-steroids;Journal of Chemical Research;2004-07
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