Volume 27, Issue 18
Isocyclic Compounds
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ChemInform Abstract: Intramolecular Hydroxycyclopropanation of ω-Vinyl Carboxylic Esters.

J. LEE

J. LEE

Dep. Chem., Univ. Ala., Tuscaloosa, AL 35487, USA

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C.-H. KANG

C.-H. KANG

Dep. Chem., Univ. Ala., Tuscaloosa, AL 35487, USA

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H. KIM

H. KIM

Dep. Chem., Univ. Ala., Tuscaloosa, AL 35487, USA

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J. K. CHA

J. K. CHA

Dep. Chem., Univ. Ala., Tuscaloosa, AL 35487, USA

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First published: April 30, 1996

Abstract

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ChemInform Abstract

The title reaction is of synthetic utility in carbocyclic ring construction. It is demonstrated that in general these reactions appear to be relatively little effected by the presence of substituents. However, if the olefin is not easily accessible as in the case of (XVI) only the corresponding intermolecular product (XVIII) is obtained. Also, neither di- nor trisubstituted alkenes give cyclized products, only intermolecular hydroxycyclopropanation takes place.

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