Tetrahedron

Synthesis and 13 C-NMR spectroscopic investigations of rhamnobioses

A Lipták, P Nánási, A Neszmélyi, H Wagner

Index: Liptak,A.; Nanasi,P.; Neszmelyi,A.; Wagner,H. Tetrahedron, 1980 , vol. 36, p. 1261

Full Text: HTML

Citation Number: 63

Abstract

A convenient method has been developed for the synthesis of all mono-and di-O-benzyl ethers of methyl α-L-rhamnopyranoside applying a new stereoselective method for the hydrogenolytic ring-cleavage of benzylidene acetals. Using the prepared dibenzyl ethers as aglycones, the (1→ 2)-,(1→ 3)-and (l→ 4)-linked rhamnosyl-rhamnose derivatives (13–15) were synthesised. Hydrogenolysis of the latter compounds and subsequent acetylation ...

Related Articles:

More Articles...