Regio- and stereoselectivity of diethylaluminum azide opening of trisubstituted epoxides and conversion of the 3° azidohydrin adducts to isoprenoid aziridines

Journal of Organic Chemistry

Volumn 68, Issue 1, 2003, Pages 75-82

  Davis, Chad E ^a   Bailey, Jessica L ^a   Lockner, Jonathan W ^a   Coates, Robert M ^a  

^a UNIVERSITY OF ILLINOIS AT URBANA CHAMPAIGN   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

STEREOSELECTIVITY;

ALUMINUM; ISOMERS; STEREOCHEMISTRY;

AROMATIC HYDROCARBONS;

2,3 EPOXYFARNESOL; 2,3 EPOXYNEROL; 6,7 EPOXYGERANYL ACETATE; ACETIC ACID DERIVATIVE; ALUMINUM DERIVATIVE; AZIDE; AZIDOHYDRIN; AZIRIDINE DERIVATIVE; DIETHYLALUMINUM AZIDE; EPOXIDE; ISOPRENOID; ISOPRENOID AZIRIDINE; TERPENE DERIVATIVE; TOLUENE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CYCLIZATION; ISOMER; REDUCTION; SILYLATION; STEREOCHEMISTRY;

AZIDES; AZIRIDINES; CATALYSIS; CYCLIZATION; EPOXY COMPOUNDS; MAGNETIC RESONANCE SPECTROSCOPY; MOLECULAR STRUCTURE; SILANES; STEREOISOMERISM; TERPENES;

EID: 0037428006     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo026506c     Document Type: Article

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