The cinnamate-based aminohalogenation provides an easy access to antimethyl 3-aryl-N-p-tosyl- and N-o-nosyl-aziridine-2-carboxylates

Arkivoc

Volumn 2003, Issue 12, 2003, Pages 56-62

  Chen, Dianjun ^a   Kim, Sun Hee ^a   Hodges, Brian ^a   Li, Guigen ^a  

^a TEXAS TECH UNIVERSITY   (United States)

Author keywords

Aminohalogenation; Aziridine; Cinnamate; Haloamine

Indexed keywords

ACETONITRILE; AZIRIDINE DERIVATIVE; CINNAMIC ACID; HALOAMINE; METHYL 3 (2 CHLOROPHENYL) N (4 TOLUENE)SULFONYLAZIRIDINE 2 CARBOXYLATE; METHYL 3 (2 NAPHTHYL) N (2 NITROBENZENE)SULFONYLAZIRIDINE 2 CARBOXYLATE; METHYL 3 (2 TOLYL) N (2 NITROBENZENE)SULFONYLAZIRIDINE 2 CARBOXYLATE; METHYL 3 (2 TOLYL) N (4 TOLUENE)SULFONYLAZIRIDINE 2 CARBOXYLATE; METHYL 3 (4 BROMOPHENYL) N (2 NITROBENZENE)SULFONYLAZIRIDINE 2 CARBOXYLATE; METHYL 3 (4 BROMOPHENYL) N (4 TOLUENE)SULFONYLAZIRIDINE 2 CARBOXYLATE; METHYL 3 (4 NITROPHENYL) N (4 TOLUENE)SULFONYLAZIRIDINE 2 CARBOXYLATE; METHYL 3 (4 TOLYL) N (2 NITROBENZENE)SULFONYLAZIRIDINE 2 CARBOXYLATE; METHYL 3 (4 TOLYL) N (4 TOLUENE)SULFONYLAZIRIDINE 2 CARBOXYLATE; METHYL 3 PHENYL N (2 NITROBENZENE)SULFONYLAZIRIDINE 2 CARBOXYLATE; POTASSIUM CARBONATE; UNCLASSIFIED DRUG;

AMINOHALOGENATION; ARTICLE; CYCLIZATION; HALOGENATION; ROOM TEMPERATURE;

EID: 3242721321     PISSN: 14246376     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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