We have been interested for some time in the nucleophilic addition reactions to carl-6 bony1 compounds , the interpretation of our kinetic data has lead us to conclude that the position of the transition state along the reaction coordinate is not the same for all reactions and depends instead upon t
Steric effect of α-hydrogens in nucleophilic addition reactions to carbonyl compounds
✍ Scribed by P. Geneste; G. Lamaty; J-P. Roque
- Publisher
- Elsevier Science
- Year
- 1970
- Tongue
- French
- Weight
- 123 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0040-4039
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📜 SIMILAR VOLUMES
As we haVe previously pointed out], the position of the Transition State along the reaction coordinate is a matter of controversy among workers in the field of nucleophilic addition reactions to carbonyl compounds. Some authors claim that the transition state is always "Reactant-like" whatever may b
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