Highly enantio- and diastereoselective one-pot methods for the synthesis of halocyclopropyl alcohols

Journal of the American Chemical Society

Volumn 131, Issue 3, 2009, Pages 954-962

  Kim, Hun Young ^a   Salvi, Luca ^a   Carroll, Patrick J ^a   Walsh, Patrick J ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALKOXIDE; ALLYL BROMIDE; AROMATIC ALDEHYDE; ASYMMETRIC SYNTHESIS; CARBENOIDS; COMPLEMENTARY METHODS; CUPRATE; CYCLOPROPANATION REACTION; CYCLOPROPYL; DIASTEREO-SELECTIVITY; DIASTEREOSELECTIVE; EFFICIENT SYNTHESIS; ENANTIO; FUNCTIONALIZED; ONE-POT METHOD; ONE-POT PROCEDURES; STARTING MATERIALS; STEREO-SELECTIVE; STEREOGENIC CENTERS; VINYLATION;

ALDEHYDES; BROMINE COMPOUNDS; COPPER COMPOUNDS; ENANTIOSELECTIVITY;

STEREOSELECTIVITY;

(3 BROMO 2,2 DIMETHYLCYCLOPROPYL)PROPAN 1 OL; 1 (2 BUTYL 3 IODOCYCLOPROPYL) 2 METHYLPROPAN 1 OL; 1 (3 ALLYL 2,2 DIMETHYLCYCLOPROPYL)PROPAN 1 OL; 1 (3 CHLORO 2,2 DIMETHYLCYCLOPROPYL)ETHANOL; 1 (7 IODOBICYCLO[4.1.0] HEPTAN 1 YL)PROPAN 1 OL; ALCOHOL DERIVATIVE; CYCLOPROPANE DERIVATIVE; CYCLOPROPANOL DERIVATIVE; UNCLASSIFIED DRUG; CYCLOPROPANE; VINYL DERIVATIVE;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CATALYSIS; CHEMICAL BOND; CHEMICAL STRUCTURE; CRYSTAL STRUCTURE; CYCLOPROPANATION; DIASTEREOISOMER; ENANTIOMER; ONE POT SYNTHESIS; PROTON NUCLEAR MAGNETIC RESONANCE; SIMMONS SMITH REACTION; ALKYLATION; CHEMISTRY; HALOGENATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STEREOISOMERISM; SYNTHESIS;

ALCOHOLS; ALKYLATION; CYCLOPROPANES; HALOGENATION; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; STEREOISOMERISM; VINYL COMPOUNDS;

EID: 61749101900     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja806989n     Document Type: Article

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