DABCO/Amberlyst® 15-Cocatalysed One-Pot Three-Component Aza-Morita–Baylis–Hillman Reaction Under Green Conditions

The one-pot multicomponent aza-Morita–Baylis–Hillman (MBH) reaction was performed under green conditions using 1,4-diazabicyclo[2.2.2]octane (DABCO) and Amberlyst® 15 as a co-catalyst, at ambient temperature and under negligible amounts of non-hazardous solvent. A number of α-methylene-β-amino acid derivatives were produced in good to excellent yields from different arylaldehydes, p-toluenesulfonamide and α,β-unsaturated carbonyl compounds. The environmental benignity of the process is accounted by the low E-factor (0.7) and high atom economy (95%) values obtained.

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Publication Details

Journal
Catalysts
Published
2024-11-29
DOI
https://doi.org/10.3390/catal14120873
Citations
1
Primary Topic
Chemistry and Chemical Engineering
Type
article
Field-Weighted Citation Impact
0.25
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article

DABCO/Amberlyst® 15-Cocatalysed One-Pot Three-Component Aza-Morita–Baylis–Hillman Reaction Under Green Conditions

Riccardo De Nittis, Matthew Vella Refalo, Giovanna Bosica
1 citations
Catalysts
Chemistry and Chemical Engineering
0.25
article

DABCO/Amberlyst® 15-Cocatalysed One-Pot Three-Component Aza-Morita–Baylis–Hillman Reaction Under Green Conditions

Riccardo De Nittis, Matthew Vella Refalo, Giovanna Bosica
article en
1 citations

Abstract

The one-pot multicomponent aza-Morita–Baylis–Hillman (MBH) reaction was performed under green conditions using 1,4-diazabicyclo[2.2.2]octane (DABCO) and Amberlyst® 15 as a co-catalyst, at ambient temperature and under negligible amounts of non-hazardous solvent. A number of α-methylene-β-amino acid derivatives were produced in good to excellent yields from different arylaldehydes, p-toluenesulfonamide and α,β-unsaturated carbonyl compounds. The environmental benignity of the process is accounted by the low E-factor (0.7) and high atom economy (95%) values obtained.

CatalystsVol. 14(12)
University of Malta (MT)
Responsible consumption and production
Openalex Percentile: Top 41%
Chemistry and Chemical Engineering
0.25
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