The Dehydration Reactions of Nitroparaffins and Aldoximes
T Mukaiyama, T Hata
Index: Mukaiyama,T.; Hata,T. Bulletin of the Chemical Society of Japan, 1960 , vol. 33, p. 1382 - 1386
Full Text: HTML
Citation Number: 8
Abstract
This reaction proceeds to the formation of disubstituted urea and furoxane through intermediates or amine and nitrile oxide which are formed by-the decomposition of the addition compound of isocyanate and aci-nitroparaffin with spontaneous evolution of carbon dioxide. The reaction of the amine with isocyanate yields di-substituted urea and furoxane is formed by the dimerization of nitrile oxide. Nitrite oxide, one of the two intermediates, was ...
Related Articles:
[Hansen, John F.; Kim, Yong In; McCrotty, Stephen E.; Strong, Scott A.; Zimmer, Douglas E. Journal of Heterocyclic Chemistry, 1980 , vol. 17, p. 475 - 479]
Natural products to drugs: natural product derived compounds in clinical trials
[Kidwai; Sapra Organic Preparations and Procedures International, 2001 , vol. 33, # 4 p. 381 - 386]
[Ganesh, Madhu; Namboothiri, Irishi N.N. Tetrahedron, 2007 , vol. 63, # 48 p. 11973 - 11983]
[Crombie, Leslie; Roughley, Brian S. Tetrahedron, 1986 , vol. 42, # 12 p. 3147 - 3156]
[Crombie, Leslie; Roughley, Brian S. Tetrahedron, 1986 , vol. 42, # 12 p. 3147 - 3156]