Synthesis and Reactivity of 1-Pyrroline-5-carboxylate Ester 1-Oxides
摘要:
Some C5 mono- and diester-substituted 1-pyrroline-1-oxides have been prepared via reductive cyclisation of the corresponding gamma-nitro carbonyl compounds. Ethyl 2-phenyl-1-pyrroline-1-oxide-5-carboxylate 5c was regioselectively alkylated at C5. Acylation of this molecule occurs exclusively on the nitrone oxygen and leads to C3 substituted pyrrolines as the result of a hetero-Cope rearrangement. (C) 2000 Elsevier Science Ltd. All rights reserved.
Synthesis and Reactivity of 1-Pyrroline-5-carboxylate Ester 1-Oxides
作者:David StC. Black、Gavin L. Edwards、Richard H. Evans、Paul A. Keller、Sean M. Laaman
DOI:10.1016/s0040-4020(00)00094-6
日期:2000.3
Some C5 mono- and diester-substituted 1-pyrroline-1-oxides have been prepared via reductive cyclisation of the corresponding gamma-nitro carbonyl compounds. Ethyl 2-phenyl-1-pyrroline-1-oxide-5-carboxylate 5c was regioselectively alkylated at C5. Acylation of this molecule occurs exclusively on the nitrone oxygen and leads to C3 substituted pyrrolines as the result of a hetero-Cope rearrangement. (C) 2000 Elsevier Science Ltd. All rights reserved.