One step from nitro to oxime: a convenient preparation of unsaturated oximes by the reduction of the corresponding vinylnitro compounds

Tetrahedron

Volumn 65, Issue 50, 2009, Pages 10377-10382

  Wang, Kewei ^a   Qian, Xuhong ^a,b   Cui, Jingnan ^a  

^a DALIAN UNIVERSITY OF TECHNOLOGY   (China)

^b EAST CHINA UNIVERSITY OF SCIENCE AND TECHNOLOGY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

1 (2 CHLORO THIAZOL 5 YLMETHYL) 1,4,5,6 TETRAHYDRO PYRIMIDINE 2 CARBALDEHYDE OXIME; 1 (2 CHLORO THIAZOL 5 YLMETHYL) 4,5 DIHYDRO 1H IMIDAZOLE 2 CARBALDEHYDE OXIME; 1 (2 CHLORO THIAZOL 5 YLMETHYL) 4,5,6,7,8,9 HEXAHYDRO 1H BENZOIMIDAZOLE 2 CARBALDEHYDE OXIME; 1 (6 CHLORO PYRIDIN 3 YLMETHYL) 1,4,5,6 TETRAHYDRO PYRIMIDINE 2 CARBALDEHYDE OXIME; 1 (6 CHLORO PYRIDIN 3 YLMETHYL) 4,5 DIHYDRO 1H IMIDAZOLE 2 CARBALDEHYDE OXIME; 1 (6 CHLORO PYRIDIN 3 YLMETHYL) 4,5,6,7,8,9 HEXAHYDRO 1H BENZOIMIDAZOLE 2 CARBALDEHYDE OXIME; 1 BENZYL 1,4,5,6 TETRAHYDRO PYRIMIDINE 2 CARBALDEHYDE OXIME; 1 BENZYL 4,5 DIHYDRO 1H IMIDAZOLE 2 CARBALDEHYDE OXIME; 1 BENZYL 4,5,6,7,8,9 HEXAHYDRO 1H BENZOIMIDAZOLE 2 CARBALDEHYDE OXIME; 1 FURAN 2 YLMETHYL 1,4,5,6 TETRAHYDRO PYRIMIDINE 2 CARBALDEHYDE OXIME; 1 FURAN 2 YLMETHYL 4,5 DIHYDRO 1H IMIDAZOLE 2 CARBALDEHYDE OXIME; 1 FURAN 2 YLMETHYL 4,5,6,7,8,9 HEXAHYDRO 1H BENZOIMIDAZOLE 2 CARBALDEHYDE OXIME; 1 PYRIDIN 2 YLMETHYL 4,5 DIHYDRO 1H IMIDAZOLE 2 CARBALDEHYDE OXIME; 1 PYRIDIN 2 YLMETHYL 4,5,6,7,8,9 HEXAHYDRO 1H BENZOIMIDAZOLE 2 CARBALDEHYDE OXIME; 1 PYRIDIN 3 YLMETHYL 4,5 DIHYDRO 1H IMIDAZOLE 2 CARBALDEHYDE OXIME; 1 PYRIDIN 3 YLMETHYL 4,5,6,7,8,9 HEXAHYDRO 1H BENZOIMIDAZOLE 2 CARBALDEHYDE OXIME; 1 THIOPHEN 2 YLMETHYL 1,4,5,6 TETRAHYDRO PYRIMIDINE 2 CARBALDEHYDE OXIME; 1 THIOPHEN 2 YLMETHYL 4,5 DIHYDRO 1H IMIDAZOLE 2 CARBALDEHYDE OXIME; 1 THIOPHEN 2 YLMETHYL 4,5,6,7,8,9 HEXAHYDRO 1H BENZOIMIDAZOLE 2 CARBALDEHYDE OXIME; ALIPHATIC COMPOUND; GLYCERYL TRINITRATE; HYDROXYL GROUP; N(6 CHLORO PYRIDIN 3 YLMETHYL)N ETHYL N' METHYL ACETAMIDINE 2 CARBALDEHYDE OXIME; OXIME DERIVATIVE; TIN CHLORIDE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; CRYSTAL STRUCTURE; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

EID: 70350714958     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2009.10.042     Document Type: Article

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