Issue 15, 1998

An efficient synthesis of analogues of unsymmetrical archaeal tetraether glycolipids

Abstract

Unsymmetrical tetraether analogues of glycolipids found in archaebacteria, possessing either two different carbohydrate units or a saccharidic moiety and a phosphate group as polar heads and a quasi-macrocyclic lipid core, are efficiently synthesized from versatile chiral building blocks.

Article information

Article type
Paper

Chem. Commun., 1998, 1571-1572

An efficient synthesis of analogues of unsymmetrical archaeal tetraether glycolipids

G. Lecollinet, R. Auzély-Velty, T. Benvegnu, D. Plusquellec, G. Lecollinet, G. Mackenzie and J. W. Goodby, Chem. Commun., 1998, 1571 DOI: 10.1039/A802338G

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