Stereochemical Control of Reductions. 9. Haptophilicity Studies with 1,1-Disubstituted 2-Methyleneacenaphthenes
Author:
Affiliation:
1. Carl A. Olson Memorial Laboratories, Department of Chemistry, Rutgers University, Newark, New Jersey 07102
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo010633b
Reference39 articles.
1. Stereochemical control of reductions. Directive effect of carbomethoxy vs. hydroxymethyl groups in catalytic hydrogenation
2. Synthesis of angularly substituted tetrahydro- and hexahydrofluorenes
3. Stereochemical control of reductions. III. Approach to group haptophilicities
4. Stereochemical control of reductions. IV. Control of hydrogenation stereochemistry by intramolecular anionic coordination to homogeneous catalysts
5. Stereochemical control of reductions. 5. Effects of electron density and solvent on group haptophilicity
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