Hetero-Cope rearrangement for the synthesis of potassium 5-tert-butyl-2-(tert-butyl-aminoxy)-benzoate, a highly water-soluble stable free radical
摘要:
The hetero-Cope rearrangement of 4-tert-butyl-phenyl-tert-butylhydroxylamine provides an easy access to the corresponding ortho-bromoaniline, converted to the new highly water-soluble nitroxide, potassium 5-tert-butyl-2-(tert-butyl-aminoxy)benzoate. The parent carboxylic acid was found to be very persistent in water at pH 1. (C) 2002 Elsevier Science Ltd. All rights reserved.
Hetero-Cope rearrangement for the synthesis of potassium 5-tert-butyl-2-(tert-butyl-aminoxy)-benzoate, a highly water-soluble stable free radical
摘要:
The hetero-Cope rearrangement of 4-tert-butyl-phenyl-tert-butylhydroxylamine provides an easy access to the corresponding ortho-bromoaniline, converted to the new highly water-soluble nitroxide, potassium 5-tert-butyl-2-(tert-butyl-aminoxy)benzoate. The parent carboxylic acid was found to be very persistent in water at pH 1. (C) 2002 Elsevier Science Ltd. All rights reserved.
Hetero-Cope rearrangement for the synthesis of potassium 5-tert-butyl-2-(tert-butyl-aminoxy)-benzoate, a highly water-soluble stable free radical
作者:Lucien Marx、André Rassat
DOI:10.1016/s0040-4039(02)00311-8
日期:2002.4
The hetero-Cope rearrangement of 4-tert-butyl-phenyl-tert-butylhydroxylamine provides an easy access to the corresponding ortho-bromoaniline, converted to the new highly water-soluble nitroxide, potassium 5-tert-butyl-2-(tert-butyl-aminoxy)benzoate. The parent carboxylic acid was found to be very persistent in water at pH 1. (C) 2002 Elsevier Science Ltd. All rights reserved.