Reductive heterocyclizations via indium/iodine-promoted one-pot conversion of 2-nitroaryl aldehydes, ketones, and imines

Tetrahedron Letters

Volumn 47, Issue 41, 2006, Pages 7295-7299

  Han, Rongbi ^a,b   Son, Kee In ^a   Ahn, Gil Hwan ^a   Jun, Young Moo ^a   Lee, Byung Min ^c   Park, Younbong ^d   Kim, Byeong Hyo ^a  

^a Kwangwoon University   (South Korea)

^b YANBIAN UNIVERSITY   (China)

^c Korea Research Institute of Chemical Technology   (South Korea)

^d Chungnam National University   (South Korea)

Author keywords

Indium and compounds; Nitro compounds; Reduction

Indexed keywords

2,1 BENZISOXAZOLE; 3 ANILINO 2 PHENYL 2H INDAZOLE; ALDEHYDE DERIVATIVE; ANILINE DERIVATIVE; HYDROXIDE; IMINE; INDIUM; IODINE; KETONE DERIVATIVE; N (2 NITROBENZYLIDINE)ANILINE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CYCLIZATION; ELECTRON TRANSPORT; INFRARED SPECTROSCOPY; MASS SPECTROMETRY; PROTON NUCLEAR MAGNETIC RESONANCE; QUANTUM YIELD; REACTION ANALYSIS; REDUCTION; SYNTHESIS;

EID: 33748309420     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.08.027     Document Type: Article

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39. 3 319.0876, found 319.0874. The crystallographic data for the structure of (4-chloro-2-phenyl-2H-indazol-3-yl)phenylamine in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 614941.