Ozonation of phenyl-substituted thiophenes
PS Bailey, HH Hwang
Index: Bailey, Philip S.; Hwang, Hank H. Journal of Organic Chemistry, 1985 , vol. 50, # 10 p. 1778 - 1779
Full Text: HTML
Citation Number: 13
Abstract
5 cis-butenediones were obtained as minor products in yields of 3-35%, depending on the aryl substituents, solvent, and temperature.'Along with this type of product, which results from electrophilic ozone attack at position 2 of the furan ring followed by loss of oxygen and 1, 2- bond cleavage, products derived from 2, 3-bond attack and cleavage were obtained.'
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]
[Ma, Chicheng; Steinmetz, Mark G.; Kopatz, Erica J.; Rathore, Rajendra Journal of Organic Chemistry, 2005 , vol. 70, # 11 p. 4431 - 4442]
[Ma, Chicheng; Steinmetz, Mark G.; Kopatz, Erica J.; Rathore, Rajendra Journal of Organic Chemistry, 2005 , vol. 70, # 11 p. 4431 - 4442]
[Ma, Chicheng; Steinmetz, Mark G.; Kopatz, Erica J.; Rathore, Rajendra Journal of Organic Chemistry, 2005 , vol. 70, # 11 p. 4431 - 4442]