Stereoselective synthesis of trifluoromethyl-substituted 1,2-diamines by aza-Michael reaction with trans-3,3,3-trifluoro-1-nitropropene

Tetrahedron

Volumn 62, Issue 34, 2006, Pages 8109-8114

  Turconi, Joël ^a   Lebeau, Luc ^a   Paris, Jean Marc ^b   Mioskowski, Charles ^a  

^a CNRS   (France)

^b Rhodia Recherches   (France)

Author keywords

3,3,3 Trifluoro 1 nitropropene; 4 Phenyl 2 oxazolidinone; Diastereoselective aza Michael addition; Perfluoroalkyl nitroalkene

Indexed keywords

3,3,3 TRIFLUORO 1 NITROPROPENE; 4 PHENYL 2 OXAZOLIDINONE; ALKANE DERIVATIVE; ALKENE DERIVATIVE; DIAMINE; OXAZOLIDINONE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL MODIFICATION; CHEMICAL REACTION KINETICS; DRUG SYNTHESIS; LOW TEMPERATURE; MICHAEL ADDITION; PRIORITY JOURNAL; QUANTUM YIELD; STEREOCHEMISTRY; TEMPERATURE DEPENDENCE; TRANS ISOMER;

TRIFLUORO;

EID: 33745727381     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.06.013     Document Type: Article

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