109171-57-5Relevant articles and documents
Cascade Michael-Aldol reaction: Efficient annulation of sulfonamide chalcones into novel cyclohexenones under solvent-free conditions
Agrawal, Nikita R.,Bahekar, Sandeep P.,Agrawal, Abhijeet R.,Sarode, Prashant B.,Chandak, Hemant S.
, p. 227 - 245 (2016/07/06)
A simple, convenient and efficient synthesis of novel sulfonamide cyclohexenones from differently substituted sulfonamide chalcones has been developed. Syntheses of cyclohexenones have been achieved via cascade Michael-Aldol reaction under solvent free condition. This process features mild and solvent-free synthesis of the titled compounds with high yields (18 examples, up to 95% yield). The synthesized scaffold is a promising intermediate for the further transformation into various heterocyclic compounds.
Synthesis and antimicrobial activities of some N-{4-[5-aryl-1- (isonicotinoyl)pyrazol-3-yl]-phenyl}-benzenesulfonamide and 3-(4- benzenesulfonylaminophenyl)-5-aryl-pyrazole-1-carboxylic acid amide
Jamode,Chandak,Bhagat
body text, p. 1169 - 1173 (2009/12/31)
A series of N-{4-[5-aryl-1-(isonicotinoyl)pyrazol-3-yl]-phenyl}- benzenesulfonamide (3a-e) and 3-(4-benzenesulfonylaminophenyl)-5-aryl-pyrazole- 1-carboxylic acid amide (4a-e) have been synthesized by refluxing N-[4-(2,3-dibromo-3-aryl-propanoyl)-phenyl]-
Studies on pyrazolines. Part III. Preparation and antimicrobial activity of 3-(4'-phenyl-sulphonamidophenyl)-5-aryl-I-acetyl/phenyi-4,5-dihydropyr azoles
Upadhyay,Dave,Parekh
, p. 413 - 414 (2007/10/02)
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