Highly diastereoselective Michael reaction under solvent-free conditions using microwaves: Conjugate addition of flavanone to its chalcone precursor

Tetrahedron Letters

Volumn 42, Issue 8, 2001, Pages 1403-1406

  Patonay, Tamás ^a   Varma, Rajender S ^b   Vass, András ^c   Lévai, Albert ^a   Dudás, József ^c  

^a UNIVERSITY OF DEBRECEN   (Hungary)

^b U S ENVIRONMENTAL PROTECTION AGENCY   (United States)

^c SZENT ISTVÁN UNIVERSITY   (Hungary)

Author keywords

Addition reactions; Chalcones; Dimers; Flavanones; Microwave heating

Indexed keywords

1,8 DIAZABICYCLO[5.4.0.]UNDEC 7 ENE; 2 HYDROXYCHALCONE; ALKENE DERIVATIVE; CHALCONE DERIVATIVE; DIMER; FLAVANONE; KETONE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CONJUGATE; CRYSTAL STRUCTURE; CYCLIZATION; DIASTEREOISOMER; DIMERIZATION; MICROWAVE RADIATION; REACTION ANALYSIS; STEREOCHEMISTRY; SYNTHESIS;

EID: 0035911022     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)02264-4     Document Type: Article

References (15)