2012
DOI: 10.1016/j.tetasy.2012.03.018
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Enantioselective synthesis of 2-amino-4H-pyrans via the organocatalytic cascade reaction of malononitrile and α-substituted chalcones

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Cited by 33 publications
(18 citation statements)
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“…2-Aminopyranopyridine-3-carbonitriles 2h-2n derived from monoenones 1h-1n were also prepared (Scheme 4) [12]. Cyclic enones 1h-1j reacted with malononitrile in the presence of triethylamine.…”
Section: Chemistrymentioning
confidence: 99%
See 1 more Smart Citation
“…2-Aminopyranopyridine-3-carbonitriles 2h-2n derived from monoenones 1h-1n were also prepared (Scheme 4) [12]. Cyclic enones 1h-1j reacted with malononitrile in the presence of triethylamine.…”
Section: Chemistrymentioning
confidence: 99%
“…Recently we have developed efficient methods for the synthesis of homochiral 2-amino-4H-pyran-3-carbonitriles [11,12]. We are interested in the effect of chiral center of these compounds on the antitubercular activity.…”
Section: Introductionmentioning
confidence: 99%
“…Fused pyran ring existing in both numerous natural products and synthetic compounds is an important heteroatom framework [1][2][3][4][5], which demonstrate great function on pharmacological activities, antibacterial, antiviral, anticoagulant, antianaphylactic, anticancer, diuretic activities, neurodegenerative disorders, and so on [6][7][8][9][10]. Recently, 2aminochromenes are found to be employed as pigments, cosmetics, and agrochemicals [11][12][13].…”
Section: Introductionmentioning
confidence: 99%
“…A cascade reaction of malononitrile and αsubstituted calcone allowed to synthesize chiral multi-substituted amino-4H-pyrane derivatives. Alkoloids were checked up as catalyst in pyrane synthesis reactions [6].…”
Section: Introductionmentioning
confidence: 99%