The Dissociative Route in the Alkaline Hydrolysis of Aryl 4-Hydroxy-β-styrenesulfonates-Reference-Cited by-同舟云学术

The Dissociative Route in the Alkaline Hydrolysis of Aryl 4-Hydroxy-β-styrenesulfonates

Published:1998-03-10 Issue:7 Volume:63 Page:2125-2129
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Cevasco Giorgio¹,Thea Sergio¹

Affiliation:

1. C.N.R., Centro di Studio per la Chimica dei Composti Cicloalifatici ed Aromatici, Dipartimento di Chimica e Chimica Industriale, Via Dodecaneso 31, 16146 Genova, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo971508w

Reference20 articles.

1. A novel dissociative mechanism in acyl group transfer from aryl 4-hydroxybenzoates in aqueous solvents

2. Participation of an Extended p-Oxo Ketene Intermediate in the Dissociative Alkaline Hydrolysis of Aryl 4-Hydroxycinnamates

3. Elimination-addition mechanisms of sulfonyl group transfer: evidence for a sulfoquinone intermediate in the hydrolysis of 2,4-dinitrophenyl 3,5-dimethyl-4-hydroxybenzenesulfonate

4. Sulfoquinones in the hydrolysis of aryl esters of o- and p-hydroxyarenesulfonic acids in alkaline aqueous solutions of dioxane

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