Cyclisation and rearrangement of N4-acylaminodeoxycytidines
作者:David Loakes、Daniel M. Brown、Stephen A. Salisbury
DOI:10.1016/s0040-4039(98)00634-0
日期:1998.5
N4-Acetylamino-2′-deoxycytidine undergoes an acid promoted cyclisation to give a 1,2,4-triazolo[4,3-c]pyrimidinone which, underbasicconditions, isomerises via a Dimroth-type rearrangement to the 1,2,4-triazolo[1,5-c]pyrimidinone.
N 4-乙酰氨基-2'-脱氧胞苷经过酸促进的环化反应,得到1,2,4-三唑并[4,3-c]嘧啶酮,该酮在碱性条件下通过Dimroth型重排异构化为1,2 ,4-三唑并[1,5-c]嘧啶酮。
Loakes, David; Brown, Daniel M.; Salisbury, Stephen A., Journal of the Chemical Society. Perkin transactions I, 1999, # 10, p. 1333 - 1337
作者:Loakes, David、Brown, Daniel M.、Salisbury, Stephen A.