Kinetics and mechanism of the conjugate hydrocyanation of .alpha.,.beta.-unsaturated ketones by the potassium cyanide-ammonium chloride system
Author:
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo00139a041
Cited by 5 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. Allylic oxidation of methyl 10‐undecenoate and nucleophilic additions to methyl 9‐oxo‐10‐undecenoate;European Journal of Lipid Science and Technology;2014-12-22
2. Conversion of unsaturated fatty acids — Nucleophilic additions to methyl (E)‐12‐Oxo‐10‐octadecenoate [1];Lipid / Fett;1996-01
3. Antibody-Catalyzed Michael Reaction of Cyanide with an .alpha.,.beta.-Unsaturated Ketone;Journal of the American Chemical Society;1995-07
4. Stereoelectronic control of intramolecular Michael addition reactions;Journal of the American Chemical Society;1983-07
5. ChemInform Abstract: KINETICS AND MECHANISM OF THE CONJUGATE HYDROCYANATION OF α,β-UNSATURATED KETONES BY THE POTASSIUM CYANIDE-AMMONIUM CHLORIDE SYSTEM;Chemischer Informationsdienst;1983-02-01
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