Dioxiranes: synthesis and reactions of methyldioxiranes
RW Murray, R Jeyaraman
Index: Murray, Robert W.; Jeyaraman, Ramasubbu Journal of Organic Chemistry, 1985 , vol. 50, # 16 p. 2847 - 2853
Full Text: HTML
Citation Number: 731
Abstract
The peroxymonosulfate-acetone system produces dimethyldioxirane under conditions permitting distillation of the dioxirane from the synthesis vessel. The same conditions were used to prepare other methyldioxiranes. Solutions of dimethyldioxirane prepared in this manner were used to study ita chemical and spectroscopic properties. The caroate-acetone system was also used to study the chemistry of in situ generated dimethyldioxirane.
Related Articles:
[Yano, Tomotake; Kuroboshi, Manabu; Tanaka, Hideo Tetrahedron Letters, 2010 , vol. 51, # 4 p. 698 - 701]
[Kuroboshi, Manabu; Yano, Tomotake; Kamenoue, Shogo; Kawakubo, Hiromu; Tanaka, Hideo Tetrahedron, 2011 , vol. 67, # 32 p. 5825 - 5831]
[Kuroboshi, Manabu; Yano, Tomotake; Kamenoue, Shogo; Kawakubo, Hiromu; Tanaka, Hideo Tetrahedron, 2011 , vol. 67, # 32 p. 5825 - 5831]
[Yakhvarov; Budnikova; Tazeev; Sinyashin Russian Chemical Bulletin, 2002 , vol. 51, # 11 p. 2059 - 2064]
A novel imido-transfer reaction of aldehydes with Ph 3 P NTs using RuCl 2 (PPh 3) 3 as catalyst
[Jain, Suman L.; Sharma, Vishal B.; Sain, Bir Tetrahedron Letters, 2004 , vol. 45, # 22 p. 4341 - 4343]