2016
DOI: 10.3998/ark.5550190.p009.449
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Chemistry of 3-carbonyl-2-methyl-4-oxo-4H-1-benzopyrans

Abstract: The review article gives a comprehensive survey of the synthesis and chemistry of the title benzopyrans covering the literature published

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Cited by 8 publications
(6 citation statements)
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“…30 Heterocyclization of the -NH-C(=X)NHNH 2 functionality of 69e with some 1,2-bifunctional electrophiles as ClCOCOCl, ClCH 2 COCl, PhCOCH 2 Br, BrCH(CN) 2 and MeCOCO 2 Na leading to the appropriate 1,2,4-triazole derivatives has also been reported. A mixture of the aldehyde 1 and hydrazine hydrate on being heated with triethylammonium bisulfate (20 mol%) at 120 °C under solvent free conditions affords the bis-hydrazone 75.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…30 Heterocyclization of the -NH-C(=X)NHNH 2 functionality of 69e with some 1,2-bifunctional electrophiles as ClCOCOCl, ClCH 2 COCl, PhCOCH 2 Br, BrCH(CN) 2 and MeCOCO 2 Na leading to the appropriate 1,2,4-triazole derivatives has also been reported. A mixture of the aldehyde 1 and hydrazine hydrate on being heated with triethylammonium bisulfate (20 mol%) at 120 °C under solvent free conditions affords the bis-hydrazone 75.…”
Section: Methodsmentioning
confidence: 99%
“…Electrophilicity at their amino substituted C-2 is somewhat reduced due to the positive resonance effect of the amino group and compares well to that at C-2 of 3-formyl-2-methylchromone 8. 2 Again, the chromones 1-4 through their amino groups can function as nucleophiles as 8 does through its 2-methyl group in the presence of an appropriate base. The amino-aldehyde 1 in this respect can be regarded as an aza-analogue of the aldehyde 8.…”
Section: Introductionmentioning
confidence: 99%
“…Polyfluorochromone-3-carboxylates 66 reacted with a variety of primary amines, under different reaction conditions, producing chromane-2,4(3Н)-diones 72 (Scheme 58). [66][67][68]72,74,75 Scheme 58…”
Section: From Chromone-3-carboxalic Acidsmentioning
confidence: 99%
“…Therefore, in recent years, continuous flow method has been an important tool for the efficiency and reusability of heterogeneous catalysts, [9][10][11][12][13][14][15][16][17] among many other synthetic organic applications. [18][19][20][21][22] Recently, Yu et al published a minreview [23] to evaluate innovations in continuous flow hydrogenation studies. In this study, recent studies on continuous flow homogeneous and heterogeneous catalysis of various organic functional groups such as alkenes and alkynes, [24][25][26][27] imines and nitro, [28,29] and carbonyl [30,31] were examined.…”
Section: Introductionmentioning
confidence: 99%