The reaction of dimethyltitanocene with N-substituted-β-lactams
摘要:
2-Methyleneazetidines have been synthesized and isolated by the reaction of beta-lactams with dimethyltitanocene, followed by chromatography on deactivated silica. Efficient conversion required that the lactam nitrogen be strongly deactivated. Methyl transfer predominated in reactions with phenyl and benzyl on the lactam nitrogen. (C) 2000 Elsevier Science Ltd. All rights reserved.
The reaction of dimethyltitanocene with N-substituted-β-lactams
作者:Isamir Martı́nez、Amy R Howell
DOI:10.1016/s0040-4039(00)00919-9
日期:2000.7
2-Methyleneazetidines have been synthesized and isolated by the reaction of beta-lactams with dimethyltitanocene, followed by chromatography on deactivated silica. Efficient conversion required that the lactam nitrogen be strongly deactivated. Methyl transfer predominated in reactions with phenyl and benzyl on the lactam nitrogen. (C) 2000 Elsevier Science Ltd. All rights reserved.