Electronic control of π-facial diastereoselection. Electrophilic additions to 7-methylenenorbornanes
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Molecular Medicine
Link
http://pubs.rsc.org/en/content/articlepdf/1991/C3/C39910000018
Reference12 articles.
1. Electronic control of stereoselectivity. 8. The stereochemical course of electrophilic additions to aryl-substituted 9-isopropylidenebenzonorbornenes
2. Geometric equivalents of enantiomers in studies of the stereochemical course of substitution at carbon. Electronic effects in nucleophilic addition to carbonyl groups and to carbocations. Virtual proof of the existence of .sigma. participation by unstrained carbon-carbon bonds
3. Hyperconjugation as a stereoinductive factor in the approach of electrophiles to trigonal carbon
4. Experimental tests of models to predict nucleophilic addition stereochemistries
5. Electronic Control of Stereoselectivity in the Metal Hydride Reductions of 1,2,3,4-Tetrahydro-1,4-methanonaphthalen-9-ones
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