Formation and structural analysis of novel dibornyl ethers

One- and two-dimensional NMR spectroscopy has been used to establish the regio- and stereochemistry of novel dibornyl ethers, obtained by acid-catalysed condensation of camphor-derived α-hydroxybornanones.

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Bibliographic Details
Published inSouth African journal of chemistry Vol. 55; no. 1; pp. 111 - 118
Main Authors Matjila, J.M., Molema, W.E., Ravindran, S.S., Duggan, A.R., Kaye, P.T.
Format Journal Article
LanguageEnglish
Published South African Chemical Institute (SACI) 01.01.2002
Subjects
Camphor derivatives
Dibornyl ethers
Short communications
Structure analysis
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Summary:One- and two-dimensional NMR spectroscopy has been used to establish the regio- and stereochemistry of novel dibornyl ethers, obtained by acid-catalysed condensation of camphor-derived α-hydroxybornanones.
ISSN:0379-4350