Vilsmeier formylation of vinylcyclopropanes II
PC Traas, H Boelens, HJ Takken
Index: Traas,P.C. et al. Recueil des Travaux Chimiques des Pays-Bas, 1976 , vol. 95, # 3 p. 57 - 66
Full Text: HTML
Citation Number: 20
Abstract
Abstract Vilsmeier formylation of vinylcyclopropanes 1 (cC 3 H 5 CR 1 [DOUBLE BOND] CHR 2, R 1= alkyl, cycloalkyl, phenyl and vinyl, R 2= hydrogen and alkyl), affords the corresponding 3-cyclopropylacroleïns in excellent yields (75-95%). Vinylcyclopropanes without an α-substituent (R 1= H) react very sluggishly and give poor yields (10-20%) with the exception of the parent compound, vinylcyclopropane (65%), and ...
Related Articles:
An Efficient, Overall [4+ 1] Cycloadditon of 1, 3??Dienes and Nitrene Precursors
[Wu, Qiong; Hu, Jian; Ren, Xinfeng; Zhou, Jianrong Chemistry - A European Journal, 2011 , vol. 17, # 41 p. 11553 - 11558]
High vibrational overtone photochemistry of 1-cyclopropylcyclobutene
[Jasinski, Joseph M.; Frisoli, Joan K.; Moore, C. Bradley Journal of Physical Chemistry, 1983 , vol. 87, p. 3826 - 3829]