2012
DOI: 10.1016/j.tetlet.2012.08.099
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A domino protocol for the efficient synthesis of structurally diverse benzothiazolylquinoline-2,5-diones and their spiro analogues

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Cited by 26 publications
(9 citation statements)
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“…Condensations of 5-amino-3-methylpyrazole ( 4 ) (Lipson and Gorobets, 2009 ; Zhong et al, 2013 ) or 5-amino-3-methyl- N -phenylpyrazole ( 21 ) (Shi et al, 2011 ) with aldehydes 1 or arylglyoxals (Petrova et al, 2014 ) and Meldrum's acid 45 under various conditions gave 5-pyrimidinones 52a and 53a , correspondingly (Figure 4 ); similar heterocycles were obtained from 2-aminobenzothiazole (Arya et al, 2012 ).…”
Section: Main Partmentioning
confidence: 78%
“…Condensations of 5-amino-3-methylpyrazole ( 4 ) (Lipson and Gorobets, 2009 ; Zhong et al, 2013 ) or 5-amino-3-methyl- N -phenylpyrazole ( 21 ) (Shi et al, 2011 ) with aldehydes 1 or arylglyoxals (Petrova et al, 2014 ) and Meldrum's acid 45 under various conditions gave 5-pyrimidinones 52a and 53a , correspondingly (Figure 4 ); similar heterocycles were obtained from 2-aminobenzothiazole (Arya et al, 2012 ).…”
Section: Main Partmentioning
confidence: 78%
“…180 Replacing Meldrum's acid with barbituric acid in this reaction using SO 3 H-functionlized halogen-free ionic liquid 3-methyl-1-(butyl-4-sulfonyl)imidazolium hydrogen sulphate ([MIM(CH 2 ) 4 …”
Section: Scheme 97mentioning
confidence: 99%
“…The present synthetic methodology involves the reaction of phenylhydrazine, with o-aminoacetophenone and cyclic ketones using nanostructured Terbium doped TiO 2 as recyclable and reusable heterogeneous catalyst. In view of medicinal importance of isocryptolepine structural framework and our research interest in the synthesis of drug-like hybrid molecules with privileged heterocyclic structures, [34][35][36][37][38][39][40][41][42][43][44][45] the present synthetic protocol is probably the first report for the synthesis of spiroannulated indolo […”
Section: Introductionmentioning
confidence: 99%