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Published in 2018 at "Chemical Research in Chinese Universities"
DOI: 10.1007/s40242-018-7320-1
Abstract: A convenient and efficient method was developed for the synthesis of 2,2′-(arylmethylene)bis(3-hydrox- ycyclohex-2-enone) derivatives via the oleylamine-catalyzed tandem Knoevenagel/Michael addition reactions of aromatic aldehydes and cyclohexane-1,3-diones. This transformation proceeded without any metal catalyst in non-toxic…
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Keywords:
michael addition;
catalyzed tandem;
oleylamine catalyzed;
tandem knoevenagel ... See more keywords
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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…
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Keywords:
bis dimedone;
dimedone derivatives;
tandem knoevenagel;
dimedone ... See more keywords
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Published in 2020 at "Synthetic Communications"
DOI: 10.1080/00397911.2020.1821226
Abstract: Abstract The stereoselective syntheses of novel trans-5-aroyl-2,4-diaryl-4,5-dihydrofuran-3-carbonitriles have been achieved via a one-pot, three-component tandem protocol involving aroyl acetonitriles, aromatic aldehydes, and imidazolium ylide in the presence of Et3N. Graphical Abstract
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Keywords:
mediated tandem;
michael cyclization;
tandem knoevenagel;
imidazolium ylide ... See more keywords