Literature DB >> 22197000

Ultrasound-assisted aza-Michael reaction in water: a green procedure.

Debasish Bandyopadhyay1, Sanghamitra Mukherjee, Luis C Turrubiartes, Bimal K Banik.   

Abstract

The conjugate addition of amines to conjugated alkenes (commonly known as aza-Michael reaction) constitutes a key step for the synthesis of various complex natural products, antibiotics, α-amino alcohols and chiral auxiliaries. Ultrasound-induced addition of several amines to α, β-unsaturated ketones, esters and nitriles has been carried out very efficiently in water as well as under solvent-free conditions. No catalysts or solid supports have been used in this method. Remarkable enhancement of reaction rate has been observed in water under ultrasound-induced method. This environmentally benign procedure has provided clean formation of the products with better selectivity. Copyright Â
© 2011. Published by Elsevier B.V.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 22197000     DOI: 10.1016/j.ultsonch.2011.11.009

Source DB:  PubMed          Journal:  Ultrason Sonochem        ISSN: 1350-4177            Impact factor:   7.491


  3 in total

1.  An expeditious green route toward 2-aryl-4-phenyl-1H-imidazoles.

Authors:  Debasish Bandyopadhyay; Lauren C Smith; Daniel R Garcia; Ram N Yadav; Bimal K Banik
Journal:  Org Med Chem Lett       Date:  2014-09-20

Review 2.  Ultrasound for Drug Synthesis: A Green Approach.

Authors:  Micheline Draye; Gregory Chatel; Romain Duwald
Journal:  Pharmaceuticals (Basel)       Date:  2020-01-31

3.  l-Proline catalyzed one-pot synthesis of polysubstituted pyridine system incorporating benzothiazole moiety via sustainable sonochemical approach.

Authors:  Hamada Mohamed Ibrahim; Wael Abdelgayed Ahmed Arafa; Haider Behbehani
Journal:  RSC Adv       Date:  2018-11-08       Impact factor: 4.036

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.