BF3·OEt2-Mediated highly regioselective S N2-type ring-opening of N-activated aziridines and N-activated azetidines by tetraalkylammonium halides

Journal of Organic Chemistry

Volumn 75, Issue 1, 2010, Pages 137-151

  Ghorai, Manas K ^a   Kumar, Amit ^a   Tiwari, Deo Prakash ^a  

^a INDIAN INSTITUTE OF TECHNOLOGY KANPUR   (India)

Author keywords

[No Author keywords available]

Indexed keywords

AZETIDINES; AZIRIDINES; CHEMICAL EQUATIONS; CHLOROAMINES; DIASTEREOSELECTIVE; HALO-AMINES; LEWIS ACID; REGIO-SELECTIVE; RING OPENING; TETRAALKYLAMMONIUM;

CHEMICAL REACTIONS;

1,2 HALOAMINE DERIVATOVE; 1,3 HALOAMINE DERIVATIVE; AZETIDINE DERIVATIVE; AZIRIDINE DERIVATIVE; HALIDE; LEWIS ACID; TETRAALKYLAMMONIUM HALIDE DERIVATIVE; UNCLASSIFIED DRUG; BORIC ACID; ETHER DERIVATIVE; HALOGENATED HYDROCARBON; QUATERNARY AMMONIUM DERIVATIVE;

ARTICLE; CHEMICAL REACTION; HALOGENATION; STEREOCHEMISTRY; SYNTHESIS; CATALYSIS; CHEMICAL STRUCTURE; CHEMISTRY; STEREOISOMERISM; STRUCTURE ACTIVITY RELATION;

AZETIDINES; AZIRIDINES; BORATES; CATALYSIS; ETHYL ETHERS; HYDROCARBONS, HALOGENATED; MOLECULAR STRUCTURE; QUATERNARY AMMONIUM COMPOUNDS; STEREOISOMERISM; STRUCTURE-ACTIVITY RELATIONSHIP;

EID: 73449110930     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo902244y     Document Type: Article

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