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• W2953109219 endingPage "1319" @default.
• W2953109219 startingPage "1315" @default.
• W2953109219 abstract "A low hazardous, one-pot, expeditious annulation involving tandem Knoevenagel, Michael and ring transformation reactions of 3-arylrhodanines, aromatic aldehydes and a mercaptoacetyl transfer agent, 2-methyl-2-phenyl-1,3-oxathiolan-5-one, diastereoselectively yields 6-mercaptopyranothiazoles. The annulation is performed using a chiral ionic liquid (Pro2SO4) as the reaction medium and catalyst, and proceeds via an isolable intermediate." @default.
• W2953109219 created "2019-06-27" @default.
• W2953109219 creator A5040745564 @default.
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• W2953109219 date "2008-09-01" @default.
• W2953109219 modified "2023-09-23" @default.
• W2953109219 title "Multicomponent reactions in chiral ionic liquids: A stereocontrolled route to mercaptopyranothiazoles" @default.
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• W2953109219 doi "https://doi.org/10.1002/jhet.5570450510" @default.
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