The Chemistry of Maleic Hydrazide. II. 1 The Course of the Michael-type Addition2
H Feuer, R Harmetz
Index: Feuer; Harmetz Journal of the American Chemical Society, 1958 , vol. 80, p. 5877,5880
Full Text: HTML
Citation Number: 16
Abstract
I ported that compound I underwent Mannich-type reactions to yield N-substituted products. Also it has been established'recently that acylation reactions lead exclusively to esters of I. When compound I was treated with methyl vinyl ketone, methyl acrylate, acrylonitrile and dimethyl itaconate in the presence of catalytic amounts of base, the monoaddition products 2- (3'-oxobutyl)-6-hydroxy-3 (2H)-pyridazinone (11), 2-(2'-carbomethoxyethyl)-6-hydroxy-3 ( ...
Related Articles:
[Hu, Yi; Chen, Zhen-Chu; Le, Zhang-Gao; Zheng, Qin-Guo Journal of Chemical Research, 2004 , # 4 p. 276 - 278]
[Puertas, Susana; Rebolledo, Francisca; Gotor, Vicente Tetrahedron, 1995 , vol. 51, # 5 p. 1495 - 1502]
First triphenylphosphine promoted reduction of maleimides to succinimides
[Pal, Bikash; Pradhan, Prasun K.; Jaisankar, Parasuraman; Giri, Venkatachalam S. Synthesis, 2003 , # 10 p. 1549 - 1552]
[Houlihan, William J.; Gogerty, John H.; Ryan, Eileen A.; Schmitt, Gemma Journal of Medicinal Chemistry, 1985 , vol. 28, # 1 p. 28 - 31]
Solvent-mediated one-pot synthesis of cyclic N-substituted imides
[Patil, Sambhaji V.; Mahale, Keshao A.; Gosavi, Kirankumar S.; Deshmukh, Ganesh B.; Patil, Nilesh S. Organic Preparations and Procedures International, 2013 , vol. 45, # 4 p. 314 - 320]