2012
DOI: 10.1016/j.tetlet.2012.01.024
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A one-pot, three-component synthesis of new pyrano[2,3-h]coumarin derivatives

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Cited by 54 publications
(29 citation statements)
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“…Since the cyclization step might occur via a Michael addition mechanism, the strong electron delocalization in 15 presumably reduced its reactivity in the presence of phloroglucinol. The reaction procedure herein used for the preparation of compounds 4 – 15 obtained with moderate to high yield was previously reported in the literature …”
Section: Resultsmentioning
confidence: 99%
“…Since the cyclization step might occur via a Michael addition mechanism, the strong electron delocalization in 15 presumably reduced its reactivity in the presence of phloroglucinol. The reaction procedure herein used for the preparation of compounds 4 – 15 obtained with moderate to high yield was previously reported in the literature …”
Section: Resultsmentioning
confidence: 99%
“…The reaction worked efficiently in refluxing MeOH, which afforded the corresponding product 4a in 60% yield ( [15][16][17]. The model reaction without the addition of any catalyst resulted in no product (Table 1, entries [18][19][20]. So the best results were obtained by carrying out the reaction in the presence of 5 mol% of SSC in refluxing MeOH.…”
Section: Resultsmentioning
confidence: 99%
“…In the presence of catalytic amounts of In(OTf) 3 , the mixture of benzil (1 mmol), benzaldehyde (1 mmol), ammonium acetate (1 mmol), benzylamine (1 mmol) were reacted in different solvents such as water, ethanol, methanol, chloroform, acetonitrile and solvent-free conditions. From these experiments, it was clearly demonstrated that solvent-free is the best condition to accomplish this reaction ( Table 2).…”
Section: Resultsmentioning
confidence: 99%