Unexpected 1,3-oxazolidine formation in the attempted oxidation of N-aryl-N-methyl substituted β-amino alcohols using pyridinium dichromate
摘要:
1,3-Oxazolidines were obtained from the reaction of N-methyl substituted beta-amino alcohols with pyridinium dichromate in dichloromethane. A single electron transfer mechanism. SET, is proposed to account for the formation of the 1,3-oxazolidines. (C) 1998 Elsevier Science Ltd. All rights reserved.
GALOUS H.; GIRARDEAU J.-F.; FARNONY C. C.; MIOCQUE M., J. HETEROCYCL. CHEM., 1981, 18, NO 3, 561-563
作者:GALOUS H.、 GIRARDEAU J.-F.、 FARNONY C. C.、 MIOCQUE M.
DOI:——
日期:——
Galons, Herve; Girardeau, Jean-Francois; Farnoux, Claude Combet, Journal of Heterocyclic Chemistry, 1981, vol. 18, p. 561 - 564
作者:Galons, Herve、Girardeau, Jean-Francois、Farnoux, Claude Combet、Miocque, Marcel
DOI:——
日期:——
Unexpected 1,3-oxazolidine formation in the attempted oxidation of N-aryl-N-methyl substituted β-amino alcohols using pyridinium dichromate
作者:Jari T. Yli-Kauhaluoma、Curtis W. Harwig、Paul Wentworth、Kim D. Janda
DOI:10.1016/s0040-4039(98)00289-5
日期:1998.4
1,3-Oxazolidines were obtained from the reaction of N-methyl substituted beta-amino alcohols with pyridinium dichromate in dichloromethane. A single electron transfer mechanism. SET, is proposed to account for the formation of the 1,3-oxazolidines. (C) 1998 Elsevier Science Ltd. All rights reserved.