Remote Exo/Endo Selectivity in Selective Monohydrolysis of Dialkyl Bicyclo[2.2.1]heptane-2,3-dicarboxylate Derivatives
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas 79409-1061
2. Center for Biotechnology and Genomics, Texas Tech University, Lubbock, Texas 79409-3132
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo100564e
Reference34 articles.
1. Hydroboration. XXX. Additions to bicyclic olefins. I. Stereochemistry of the hydroboration of norbornene, 7,7-dimethylnorbornene, and related bicyclic olefins. Steric effects in the 7,7-dimethylnorbornyl system
2. Exo-endo relative reactivities in three representative U-shaped systems. Exo-endo rate ratio in solvolysis as a steric phenomenon
3. Additions to bicyclic olefins. V. Effect of 7,7-dimethyl substituents on the stereochemistry and rates of cyclic additions to norbornenes
4. Torsional Effects in Polycyclic Systems. II. The Stereochemistry of Attack and Departure in Norbornane Derivatives
5. Nonplanar alkenes and carbonyls: a molecular distortion which parallels addition stereoselectivity
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