Unknown

Dataset Information

0

Participation of alkoxy groups in reactions of acetals: violation of the reactivity/selectivity principle in a Curtin-Hammett kinetic scenario.


ABSTRACT: Nucleophilic substitution reactions of acetals having benzyloxy groups four carbon atoms away can be highly diastereoselective. The selectivity in several cases increased as the reactivity of the nucleophile increased, in violation of the reactivity/selectivity principle. The increase in selectivity with reactivity suggests that multiple conformational isomers of reactive intermediates can give rise to the products.

SUBMITTER: Garcia A 

PROVIDER: S-EPMC4702254 | biostudies-literature | 2015 Oct

REPOSITORIES: biostudies-literature

altmetric image

Publications

Participation of alkoxy groups in reactions of acetals: violation of the reactivity/selectivity principle in a Curtin-Hammett kinetic scenario.

Garcia Angie A   Sanzone Jillian R JR   Woerpel K A KA  

Angewandte Chemie (International ed. in English) 20150819 41


Nucleophilic substitution reactions of acetals having benzyloxy groups four carbon atoms away can be highly diastereoselective. The selectivity in several cases increased as the reactivity of the nucleophile increased, in violation of the reactivity/selectivity principle. The increase in selectivity with reactivity suggests that multiple conformational isomers of reactive intermediates can give rise to the products. ...[more]

Similar Datasets

| S-EPMC9127809 | biostudies-literature
| S-EPMC6713862 | biostudies-other
| S-EPMC6007354 | biostudies-literature
| S-EPMC7182504 | biostudies-literature
| S-EPMC3030639 | biostudies-literature
| S-EPMC4725468 | biostudies-other
| S-EPMC7337985 | biostudies-literature
| S-EPMC7331977 | biostudies-literature
| S-EPMC5273863 | biostudies-literature
| S-EPMC2570586 | biostudies-literature