Reactions of carbonyl compounds in basic solutions. Part 12. The mechanism of the alkaline hydrolysis of 3-substituted phenyl 2-acetyl- and 2-benzoyl-benzoates
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1990/P2/P29900001805
Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Kinetics and Mechanism of the Reactions of S-2,4-Dinitrophenyl 4-Substituted Thiobenzoates with Secondary Alicyclic Amines;The Journal of Organic Chemistry;2005-08-24
2. Controlled Release of Perfumery Alcohols by Neighboring-Group Participation. Comparison of the Rate Constants for the Alkaline Hydrolysis of 2-Acyl-, 2-(Hydroxymethyl)-, and 2-Carbamoylbenzoates;Helvetica Chimica Acta;2003-08
3. Controlled release of perfumery alcohols by alkaline hydrolysis of 2-formyl- and 2-acetylbenzoates and their corresponding phthalides;Journal of the Chemical Society, Perkin Transactions 2;2001
4. Substituent Effects on the Base-Catalysed Hydrolysis of Phenyl Esters of para-Substituted Benzoic Acids;Collection of Czechoslovak Chemical Communications;2000
5. Reactions of Carbonyl Compounds in Basic Solutions. Part29.1 The Alkaline Hydrolysis of UnsaturatedLactones;Journal of Chemical Research;1997
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