Stereoselective synthesis of 3,4,5,6-tetrasubstituted (1R,2R)-diaminocyclohexanes by zirconium-promoted reductive cyclisation

Synthesis

Volumn , Issue 7, 2003, Pages 1083-1086

  Grilli, Stefano ^a   Martelli, Gianluca ^a   Savoia, Diego ^a   Zazzetta, Carla ^a  

^a UNIVERSITY OF BOLOGNA   (Italy)

Author keywords

Alkenes; Amines; Asymmetric synthesis; Chiral auxiliaries; Cyclisations; Zirconium

Indexed keywords

MIXTURES; NITROGEN COMPOUNDS; SYNTHESIS (CHEMICAL);

PROTONATION;

ZIRCONIUM;

CYCLOHEXANE DERIVATIVE; DIAMINOCYCLOHEXANE DERIVATIVE; DIPHENYLETHYLAMINO 1,7 OCTADIENE DERIVATIVE; DIPHENYLETHYLAMINODIPHENYL 1,7 OCTADIENE; ETA2 (1 BUTENE)ZIRCONOCENE; PHENETHYLAMINE; PHENYL GROUP; UNCLASSIFIED DRUG; VINYL DERIVATIVE; ZIRCONIUM; ZIRCONOCENE;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; CYCLIZATION; DIASTEREOISOMER; PROTON TRANSPORT; REDUCTION; STEREOCHEMISTRY; SYNTHESIS;

EID: 0038695072     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-39170     Document Type: Article

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