1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU)-promoted efficient and versatile aza-Michael addition
摘要:
A convenient and versatile method was developed for aza-Michael addition using a substoichiometric amount of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). Various nitrogen nucleophiles were efficiently introduced to a,a-unsaturated carbonyl compounds employing 0.5 equiv of DBU. Furthermore, other heteroatomic nucleophiles could also be introduced successfully under the same reaction conditions. (c) 2006 Elsevier Ltd. All rights reserved.
Central nervous system agents. 1. Synthesis of diphenyl-tert-aminopropanols
作者:Robert B. Moffett、Richard E. Strube、Louis Skaletzky
DOI:10.1021/jm00293a018
日期:1971.11
1,8-Diazabicyclo[5.4.0]undec-7-ene (DBU)-promoted efficient and versatile aza-Michael addition
作者:Chang-Eun Yeom、Mi Jeong Kim、B. Moon Kim
DOI:10.1016/j.tet.2006.11.037
日期:2007.1
A convenient and versatile method was developed for aza-Michael addition using a substoichiometric amount of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). Various nitrogen nucleophiles were efficiently introduced to a,a-unsaturated carbonyl compounds employing 0.5 equiv of DBU. Furthermore, other heteroatomic nucleophiles could also be introduced successfully under the same reaction conditions. (c) 2006 Elsevier Ltd. All rights reserved.
Potential Hypotensive Compounds: Substituted 3-Aminopropionates and 3-Aminopropionohydroxamic Acids