Lewis acid-promoted rearrangement of 2,3-epoxy alcohol derivatives: Stereochemical control and selective formation of two types of chiral quaternary carbon centers from the single carbon skeleton

Journal of Organic Chemistry

Volumn 71, Issue 14, 2006, Pages 5191-5197

  Kita, Yasuyuki ^a   Matsuda, Satoshi ^a   Inoguchi, Ryoko ^a   Ganesh, Jnaneshwara K ^a   Fujioka, Hiromichi ^a  

^a OSAKA UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CARBONYL COMPOUNDS; LEWIS ACID; QUATERNARY CARBON CENTERS; STEREOCHEMICAL CONTROL;

ACYLATION; ALCOHOLS; CARBONYLATION; CHELATION; DERIVATIVES; MOLECULAR ORIENTATION; REACTION KINETICS; SUBSTITUTION REACTIONS;

STEREOCHEMISTRY;

2,3 EPOXY ALCOHOL DERIVATIVE; CARBON; EPOXIDE; LEWIS ACID; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; PROTON NUCLEAR MAGNETIC RESONANCE; STEREOCHEMISTRY; SYNTHESIS;

ALCOHOLS; CARBON; EPOXY COMPOUNDS; KETONES; MOLECULAR STRUCTURE; STEREOISOMERISM; TIN COMPOUNDS;

EID: 33745700327     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0604080     Document Type: Article

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