The consecutive [2+2] cycloaddition-ring expansion route to diastereomeric 1,4-diazepin-5-ones from imino-ketenimines. Alternative intramolecular transamidation of β-lactams

Tetrahedron

Volumn 61, Issue 6, 2005, Pages 1531-1537

  Alajarín, Mateo ^a   Vidal, Angel ^a   Tovar, Fulgencio ^a  

^a UNIVERSITY OF MURCIA   (Spain)

Author keywords

Azetidinones; Cycloadditions; Diazepinones; Ketenimines; Transamidation

Indexed keywords

3 (4 BROMOPHENYL) 6 METHYL 6 PHENYLHEXAHYDRO 1,4 DIAZEPIN 5 ONE; 6 METHYL 7 (4 NITROPHENYL) 6 PHENYLHEXAHYDRO 1,4 DIAZEPIN 5 ONE; 7 (3,5 DIMETHOXYPHENYL) 6 METHYL 6 PHENYLHEXAHYDRO 1,4 DIAZEPIN 5 ONE; 7 (4 CHLOROPHENYL) 6 METHYL 6 PHENYLHEXAHYDRO 1,4 DIAZEPIN 5 ONE; ACID; BETA LACTAM DERIVATIVE; CARBON; DIAZEPINE DERIVATIVE; ETHYLENE; IMIDAZOLE DERIVATIVE; KETENE DERIVATIVE; METHYL GROUP; NITROGEN; PHENYL GROUP; UNCLASSIFIED DRUG;

AMIDATION; ARTICLE; ATOM; CATALYSIS; CYCLOADDITION; HYDROLYSIS; MOLECULE; PRIORITY JOURNAL;

EID: 12444333501     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.11.069     Document Type: Article

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