Photoinduced molecular transformations. Part 154. On the mechanism of the formation of the 5-iodopentyl formate in the photolysis of cyclopentanol hypoiodite in solution in the presence of mercury(II) oxide-iodine.
作者:Hiroshi Suginome、Hisanori Senboku
DOI:10.1016/s0040-4020(01)89319-4
日期:1994.1
18O-labelling experiments established that the formation of 5-iodopentyl formate in the photolysis of cyclopentanol hypoiodite in the presence of excess mercury(II) oxide-iodine in benzene involves the following pathway: a) a β-scission of a cyclopentyloxy radical to rearrange to a primary 5-oxopentyl radical, which generates the corresponding carbocation by a metal ion-assisted one-electron oxidation;
Photoinduced transformations. Part 73. Transformations of five- (and six-) membered cyclic alcohols into five- (and six-) membered cyclic ethers - a new method of a two-step transformation of hydroxy steroids into oxasteroids
作者:Hiroshi Suginome、Shinji Yamada
DOI:10.1021/jo00194a015
日期:1984.10
Alkoxyl radicals from alcohols I. The hypoiodite reaction of cyclopentanol: evidence for sequential rather than competitive reaction pathways
作者:John L. Courtneidge
DOI:10.1016/s0040-4039(00)79598-0
日期:1992.5
The representative photostimulated hypoiodite reaction of cyclopentanol with mercury(II) oxide and iodine gives products formed by a sequence of iodoaldehyde formation, followed by consumption to give Baeyer-Villiger and hydrolysis products.
Hiroshi Suginome, Hisanori Senboku, Tetrahedron, 50 (1994) N 46, S 13101-13112
作者:Hiroshi Suginome, Hisanori Senboku
DOI:——
日期:——
Suginome, Hiroshi; Wang, Jian Bo, Journal of the Chemical Society. Perkin transactions I, 1990, # 10, p. 2825 - 2829