1,4-Dehydrochlorination of α-chloroimines as a suitable procedure for the synthesis of unactivated 2-aza-1,3-dienes and 3-aza-1,3,5-trienes
N-Benzyl and N-allyl α-chloroimines were dehydrochlorinated in a 1,4-fashion to afford the corresponding 2-aza-1,3-dienes and 3-aza-1,3,5-trienes, respectively.
De Kimpe, Norbert,Yao, Zi-Peng,Boeykens, Marc,Nagy, Milan
A new synthesis of N-(α-methoxyarylmethyl)-2,2-dimethylaziridines is presented. Different benzaldehydes were converted into the corresponding imines upon reaction with 2-bromo-2-methylpropylamine. Treatment of the latter imines with sodium methoxide affor
D'hooghe, Matthias,Hofkens, Arn,De Kimpe, Norbert
p. 1137 - 1139
(2007/10/03)
Dehalogenation of α-Halo Aldehydes via α-Halo Aldimines and 2-Aza-1,3-dienes
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De Kimpe, Norbert,Nagy, Milan,Boeykens, Marc,Schueren, Danny van der
p. 5761 - 5764
(2007/10/02)
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