123743-15-7Relevant articles and documents
Synthesis of 5-aryl-2-piperidino-5H-chromeno[3,4-c]pyridine-1-carbonitriles
Venkati,Reddy, S. Satyanarayana,Swamy,Ravikumar,Krupadanam, G. L. David
scheme or table, p. 355 - 364 (2012/06/29)
4-Chloro-2-aryl-2H-3-chromenecarbaldehydes 3a-g on reaction with malononitrile in ethanol in the presence of piperidine gave 5-aryl-2-piperidino- 5H-chromeno[3,4-c]pyridine-1-carbonitriles 4a-g in good yields. ARKAT-USA, Inc.
Highly diastereoselective Michael reaction under solvent-free conditions using microwaves: Conjugate addition of flavanone to its chalcone precursor
Patonay, Tamás,Varma, Rajender S.,Vass, András,Lévai, Albert,Dudás, József
, p. 1403 - 1406 (2007/10/03)
Microwave-assisted reaction of 2′-hydroxychalcones in the presence of DBU resulted in the formation of hitherto unknown dimers by conjugate addition of the intermediate cyclic ketone to the starting enone.
Simple technics for isomerization of 2'-hydroxychalcones to flavanones: Use of silica gel, ethylenediamine and hydroxylamine hydrochloride
Bagade, M B,Thool, A W,Lokhande, P D,Ghiya, B J
, p. 973 - 975 (2007/10/02)
2'-Hydroxychalcones (1) are isomerized to flavanones (2) by treatment with silica gel, ethylenediamine or hydroxylamine hydrochloride at low temperatures.