1,5-Benzoheteroazepines through eco-friendly general condensation reactions

Tetrahedron Letters

Volumn 52, Issue 38, 2011, Pages 4827-4834

  Nardi, Monica ^a   Cozza, Annalisa ^a   Maiuolo, Loredana ^a   Oliverio, Manuela ^b   Procopio, Antonio ^b  

^a UNIVERSITY OF CALABRIA   (Italy)

^b University of Catanzaro Magna Graecia   (Italy)

Author keywords

Benzodiazepine; Benzooxazepine; Benzothiazepine; Erbium(III) triflate; Microwave

Indexed keywords

2 AMINOPHENOL; 2 AMINOTHIOPHENOL; 2 METHYL 2,4 DI (4 METHOXYPHENYL) 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE; 2 METHYL 2,4 DI (4 NITROPHENYL) 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE; 2 METHYL 2,4 DI (4 TOLYL) 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE; 2 METHYL 2,4 DIPHENYL 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE; 2 PHENYL 4 (2 HYDROXYPHENYL) 2,3 DIHYDRO 1H 1,4 BENZODIAZEPINE; 2 PHENYL 4 (2 HYDROXYPHENYL) 2,3 DIHYDRO 1H 1,4 BENZOTHIAZEPINE; 2,2,4 TRIMETHYL 2,3 DIHYDRO 1H 1,4 BENZOOXAZEPINE; 2,2,4 TRIMETHYL 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE; 2,2,4 TRIMETHYL 7 NITRO 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE; 2,2,4 TRIMETHYL 8 NITRO 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE; 2,2,4,6 TETRAMETHYL 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE; 2,2,4,7 TETRAMETHYL 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE; 2,2,4,8 TETRAMETHYL 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE; 2,2,4,9 TETRAMETHYL 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE; 2,4 DIETHYL 2 METHYL 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE; 2,4 DIMETHYL 1H 1,5 BENZODIAZEPINE; 2,4 DIPHENYL 2,3 DIHYDRO 1H 1,4 BENZODIAZEPINE; 2,4 DIPHENYL 2,3 DIHYDRO 1H 1,4 BENZOTHIAZEPINE; 3 METHYL 2,2,4 TRIETHYL 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE; 4 (2 HYDROXYPHENYL), 2 (4 METHOXYPHENYL) 2,3 DIHYDRO 1H 1,4 BENZODIAZEPINE; 4 (2 HYDROXYPHENYL), 2 (4 METHOXYPHENYL) 2,3 DIHYDRO 1H 1,4 BENZOTHIAZEPINE; ACETONE; BENZODIAZEPINE DERIVATIVE; BENZOTHIAZEPINE DERIVATIVE; CHALCONE DERIVATIVE; ERBIUM; KETONE; PHENYLENEDIAMINE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; DRUG STRUCTURE; DRUG SYNTHESIS; MICROWAVE IRRADIATION; NUCLEOPHILICITY; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SUBSTITUTION REACTION;

EID: 84860389966     PISSN: 00404039     EISSN: 18733581     Source Type: Journal    
DOI: 10.1016/j.tetlet.2011.06.029     Document Type: Article

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