Simultaneous reduction of the nitro group and the azide group in o-nitrophenylazide induced by the TiCl4/Sm system: A novel synthesis of 2,3-dihydro-1H-1,5-benzodiazepines

Tetrahedron Letters

Volumn 42, Issue 1, 2001, Pages 73-75

  Zhong, Weihui ^a   Zhang, Yongmin ^a,b   Chen, Xiaoyuan ^c  

^a ZHEJIANG UNIVERSITY   (China)

^b INSTITUTE OF GEOLOGY AND GEOPHYSICS   (China)

^c JISHOU UNIVERSITY   (China)

Author keywords

2,3 dihydro 1H 1,5 benzodiazepine; Azide; Nitro group; Reductive cyclization; Samarium; Titanium tetrachloride

Indexed keywords

2 NITROPHENYL AZIDE; 2,3 DIHYDRO 1H 1,5 BENZODIAZEPINE DERIVATIVE; AZIDE; BENZODIAZEPINE DERIVATIVE; NITRO DERIVATIVE; TITANIUM DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; DRUG STRUCTURE; DRUG SYNTHESIS; REACTION ANALYSIS; REDUCTION;

EID: 0035191078     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)01888-8     Document Type: Article

References (24)