The Oximes of alpha, beta-Unsaturated Ketones and the Beckmann Rearrangement. II
AH Blatt, JF Stone
Index: Blatt; Stone Journal of the American Chemical Society, 1931 , vol. 53, p. 4134,4142
Full Text: HTML
Citation Number: 7
Abstract
In a recent article 'we presented evidence to show that the oximes of certain a, p-unsaturated ketones possessed the syn2 configuration (I) and underwent a trans shift in the Beckmann rearrangement, and that the closely related and isomeric isoxazolines (11) were not formed through a
Related Articles:
[Mendes, Eduarda; Furtado, Tania; Neres, Joao; Iley, Jim; Jarvinen, Tomi; Rautio, Jarkko; Moreira, Rui Bioorganic and Medicinal Chemistry, 2002 , vol. 10, # 3 p. 809 - 816]
[Mendes, Eduarda; Furtado, Tania; Neres, Joao; Iley, Jim; Jarvinen, Tomi; Rautio, Jarkko; Moreira, Rui Bioorganic and Medicinal Chemistry, 2002 , vol. 10, # 3 p. 809 - 816]
Photochemical cleavage and release of carboxylic acids from α-keto amides
[Ma, Chicheng; Steinmetz, Mark G.; Kopatz, Erica J.; Rathore, Rajendra Journal of Organic Chemistry, 2005 , vol. 70, # 11 p. 4431 - 4442]
Photochemical cleavage and release of carboxylic acids from α-keto amides
[Ma, Chicheng; Steinmetz, Mark G.; Kopatz, Erica J.; Rathore, Rajendra Journal of Organic Chemistry, 2005 , vol. 70, # 11 p. 4431 - 4442]
Photochemical cleavage and release of carboxylic acids from α-keto amides
[Ma, Chicheng; Steinmetz, Mark G.; Kopatz, Erica J.; Rathore, Rajendra Journal of Organic Chemistry, 2005 , vol. 70, # 11 p. 4431 - 4442]