Nitromethane 1a or nitroethane 1b react with electrophilic alkenes 2a-i RCH=C(CN)(Y) with Y=CO2R', CN, CONH2 adsorbed on alumina to give selectively at room temperature or under focused microwave irradiation new Michael monoadducts 5 (two diastereoisomers) or 6 (four diastereoisomers) after a few minutes. It is possible to obtain only two diastereoisomers of 6 by reaction of the corresponding nitroalkene and methylcyanoacetate in the presence of catalytic amounts of piperidine. Mechanisms are proposed. Some examples of addition of nitroalkanes with electron-deficient alkynes in dry media coupled with microwave irradiation conditions are also described. (C) 2003 Elsevier Science Ltd. All rights reserved.
Methyl β-(Benzotriazol-l-yl) vinyl Ketone: A New p-Acetylvinyl Cation Equivalent
作者:Alan R. Katritzky、Torsten Blitzke、Jianqing Li
DOI:10.1080/00397919608003793
日期:1996.10
Abstract A simple and efficient two-step approach to methyl β-(benzotriazol-1-yl)vinyl ketone 7 is described. The synthetic utility of compound 7 has been demonstrated by nucleophilic substitutions of the benzotriazolyl group with a range of nucleophiles. Thus, methyl β-(benzotriazol-1-yl)vinyl ketone provides a new β-acetylvinyl cation equivalent.