Data published in the last 10 years on the use of the aza-Michael reaction in organic
synthesis are described systematically. The attention is focused on environmentally friendly …

Aza-Michael reaction is a simple and accessible addition reaction performed at moderate
temperature, possibly without a catalyst and without releasing by-products. Its versatility …

Aza-Michael addition is one of the most exploited reactions in organic chemistry. It is
regarded as one of the most popular and efficient methods for the creation of the carbon …

A highly porous metal–organic framework (MOF-199) was synthesized from the reaction of
copper nitrate trihydrate and 1, 3, 5-benzenetricarboxylic acid by solvothermal method, and …

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 …

Significant rate acceleration of the aza-Michael reaction in water - ScienceDirect Skip to main
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A task-specific ionic liquid, 1, 8-diazabicyclo [5.4. 0]-undec-7-en-8-ium acetate has been
successfully used as a catalyst for aza-conjugate addition of aliphatic or aromatic amines to …

Whereas the beneficial effect of water on reaction rate is decreased with an increase of the
reactant′ s hydrophobicity, we report here that the use of glycerol as solvent was able to …

Highly efficient and environmentally benign aza-Michael additions of amines to α, β-
unsaturated compounds catalyzed by β-cyclodextrin in water to produce the corresponding …

The one-pot three-component reaction of aryl aldehydes with hydroxylamine hydrochloride
and ethyl 3-oxobutanoate/ethyl 4-chloro-3-oxobutanoate/ethyl 3-oxo-3-phenylpropanoate in …