Enantiopure 2-aryl-2-methyl cyclopentanones by an asymmetric chelation-controlled Heck reaction using aryl bromides: increased preparative scope and effect of ring size on reactivity and selectivity

Tetrahedron Asymmetry

Volumn 19, Issue 9, 2008, Pages 1120-1126

  Datta, Gopal K ^a   Nordeman, Patrik ^a   Dackenberg, Jakob ^a   Nilsson, Peter ^a   Hallberg, Anders ^a   Larhed, Mats ^a  

^a UPPSALA UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

2 (1 METHYLPYROLIDINE 2 YLMETHOXY)CYCLOHEX 2 ENYLBENZENE; 2 (1 METHYLPYRROLIDINE 2 YLMETHOXY)CYCLOHEX 2 ENYLMETHYLBENZENE; 2 (1 METHYLPYRROLIDINE 2 YLMETHOXY)CYCLOHEX 2 ENYLNAPHTHALENE; ALKENE; BROMIDE; CYCLOPENTANONE DERIVATIVE; IODIDE; PALLADIUM; PYRROLIDINE DERIVATIVE; VINYL ETHER 1 METHYL 2 (CYCLOHEX 1 ENYLOXYMETHYL) PYRROLIDINE;

ARTICLE; ARYLATION; CATALYSIS; CHELATION; CHEMICAL STRUCTURE; ENANTIOMER; HECK REACTION; HYDROLYSIS; MICROWAVE COOKING; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 43649099893     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2008.04.004     Document Type: Article

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