Stereochemistry of the mercurideboronation at a saturated primary carbon atom: Inversion of configuration
- 1 January 1974
- journal article
- research article
- Published by Wiley in Bulletin des Sociétés Chimiques Belges
- Vol. 83 (9-10), 333-335
- https://doi.org/10.1002/bscb.19740830903
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Stereochemistry of reactions at carbon-transition metal .sigma. bonds. .pi.-Cyclopentadienyldicarbonyliron erythro-and threo-3,3-dimethylbutyl-1,2-d2Journal of the American Chemical Society, 1974
- Stereochemistry of reactions occurring at iron-carbon .sigma. bondsJournal of the American Chemical Society, 1971
- Organoboranes : XI. A study of the mercuration of organoboranes containing secondary alkyl groupsJournal of Organometallic Chemistry, 1971
- Base-induced bromination of tri-exo-norbornylborane: an electrophilic substitution with predominant inversion of configurationJournal of the Chemical Society D: Chemical Communications, 1971
- Organoboranes. X. Fast reaction of organoboranes with mercuric acetate. Convenient procedure for the conversion of terminal olefins into alkylmercuric salts via hydroboration-mercurationJournal of the American Chemical Society, 1970
- Conformational Isomerism in 1-Substituted Derivatives of 3,3-DimethylbutaneJournal of the American Chemical Society, 1967
- Studies in Magnetic Nonequivalence. The Conformation of Two 1-Substituted 1,2-DibromoethanesJournal of the American Chemical Society, 1966
- Hydroboration. XVIII. The Reaction of Diisopinocampheylborane with Representative cis-Acyclic, Cyclic, and Bicyclic Olefins. A Convenient Systhesis of Optically Active Alcohols and Olefins of High Optical Purity and Established ConfigurationJournal of the American Chemical Society, 1964
- Hydroboration. XI. The Hydroboration of Acetylenes—A Convenient Conversion of Internal Acetylenes into cis-Olefins and of Terminal Acetylenes into AldehydesJournal of the American Chemical Society, 1961