Author:
Anvia Fredrick,Bowden Keith,El Kaissi Faiq A.,Saez Victoria
Publisher
Royal Society of Chemistry (RSC)
Cited by
14 articles.
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1. ChemInform Abstract: Reactions of Carbonyl Compounds in Basic Solutions. Part 13. The Mechanism of the Alkaline Hydrolysis of 3-(3-Substituted Phenoxy) phthalides, -3-methylphthalides, -3-phenylphthalides, -naphthalides, - 3-phenylnaphthalides, and -phena;ChemInform;2010-08-23
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. Stereoselective synthesis of 3-substituted phtalides via asymmetric transfer hydrogenation using well-defined ruthenium catalysts under neutral conditions;Tetrahedron Letters;2001-03
4. 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
5. (β-Amino alcohol)(arene)ruthenium(II)-Catalyzed Asymmetric Transfer Hydrogenation of Functionalized Ketones − Scope, Isolation of the Catalytic Intermediates, and Deactivation Processes;European Journal of Organic Chemistry;2001-01