Tandem Knoevenagel–Michael reactions in aqueous diethylamine medium: A greener and efficient approach toward bis-dimedone derivatives
Sign Up to like & getrecommendations! Published in 2017 at "Arabian Journal of Chemistry"
DOI: 10.1016/j.arabjc.2014.04.008
Abstract: Abstract Diethylamine catalyzed tandem Knoevenagel–Michael reactions have been carried out in aqueous medium as an efficient, greener and cost effective process for the simple one-pot synthesis of bis-dimedone derivatives. Reaction of substituted aromatic aldehyde (1… read more here.
Keywords: bis dimedone; dimedone derivatives; tandem knoevenagel; dimedone ... See more keywords
Exploration of experimental and theoretical properties of 5,5-dimethyl 3-amino-cyclohex-2-en-1-one(AMINE DIMEDONE) by DFT/TD-DFT with ethanol and DMSO as solvents and Molecular Docking studies
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DOI: 10.1016/j.molliq.2021.116551
Abstract: Abstract 5,5-dimethyl 3-amino-cyclohex-2-en-1-one (AMINE DIMEDONE or 3ADCE)is one of the derivatives of 5,5-Dimethyl-1,3 cyclohexanedione (DIMEDONE) and it is one of the β-Enaminones, employed for the synthesis of nitrogen containing compounds. We have examined the titled… read more here.
Keywords: dimedone; one amine; amino cyclohex; cyclohex one ... See more keywords
Application of Dimedone Enamines as Protecting Groups for Amines and Peptides.
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DOI: 10.1021/acs.orglett.0c00586
Abstract: A simple protocol for the protection of amines was realized through a base-catalyzed one-pot reaction of dimedone, β-nitroalkene, and amine. Employing this strategy, a variety of amines/amino acids were protected in excellent yields. These acid/base… read more here.
Keywords: groups amines; application dimedone; dimedone enamines; protecting groups ... See more keywords