A convenient synthesis of 1,2,3,4-tetrahydroisoquinolin-3-ones and evidence for the participation of a quinone methide intermediate in the thermolysis of mixtures of isochroman-3-ones and ureas
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference8 articles.
1. Reaction of 6,7-dimethoxy-3-isochromanone with hydrazine
2. Reaction of 6,7-dimethoxy-3-isochromanone with hydrazine: a reinvestigation
3. Active-site-directed inhibition of .alpha.-chymotrypsin by deaminatively produced carbonium ions: an example of suicide or enzyme-activated-substrate inhibition
Cited by 9 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. Cationic ring-opening polymerization of 3-isochromanone through formation of benzyl cationic intermediate and its Friedel-Crafts reaction;Journal of Polymer Science Part A: Polymer Chemistry;2009-04-15
2. Stereoselective Synthesis of Novel Highly Substituted Isochromanone and Isoquinolinone-Containing Exocyclic Tetrasubstituted Alkenes;The Journal of Organic Chemistry;2009-02-05
3. A New Synthesis of 3-Isochromanone Derivatives Based on the Reaction ofo-Acylbenzyllithiums with Ethyl Chloroformate;Bulletin of the Chemical Society of Japan;1994-02
4. 3(2H)-Isoquinolinones and Their Saturated Derivatives;Advances in Heterocyclic Chemistry Volume 52;1991
5. Preparation of novel 4-substituted 6-methoxy-, 6,7-dimethoxy-, and 6,7-(methylenedioxy)isochroman-3-ones. 2;The Journal of Organic Chemistry;1990-03
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