A convenient approach to enantioenriched cyclopropanes bearing electron-withdrawing functionalities

Synthesis

Volumn , Issue 9, 2009, Pages 1473-1476

  Krawczyk, Henryk ^a   Wa̧sek, Katarzyna ^a   Kȩdzia, Jacek ^a  

^a LODZ UNIVERSITY OF TECHNOLOGY   (Poland)

Author keywords

Chiral allylic alcohols; Cyclopropanation; Intramolecular nucleophilic substitution; Stereoselective synthesis

Indexed keywords

CHIRAL ALLYLIC ALCOHOLS; CYCLOPROPANATION; ELECTRON WITHDRAWING GROUP; ELECTRONWITHDRAWING; FUNCTIONALIZED; INTRAMOLECULAR NUCLEOPHILIC SUBSTITUTION; STEREOSELECTIVE SYNTHESIS;

PROPANE; STEREOCHEMISTRY; UNSATURATED COMPOUNDS;

STEREOSELECTIVITY;

2 N BUTYLCYCLOPROPANENITRILE; CYCLOPROPANE DERIVATIVE; DIETHYL 2 N BUTYLCYCLOPROPANEPHOSPHONATE; ETHYL N BUTYLCYCLOPROPANECARBOXYLATE; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; PHOSPHORUS NUCLEAR MAGNETIC RESONANCE; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 67650034232     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0028-1088034     Document Type: Article

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