Issue 3, 1983

Synthesis of novel chiral macrocyclic ligands bearing methyl 4,6-O-benzylidene-α-D-mannopyranoside

Abstract

O-Alkylation of methyl 4,6-O-benzylidene-α-D-mannopyranoside with t-butyl bromoacetate under phase-transfer conditions, followed by reduction and tosylation leads to an intermediate which was used in the formation of the two diaza-crown ethers (3a) and (3b)via condensation with 1,8-diamino-3,6-dioxaoctane in the presence of KF–Al2O3 and N,N-bisethoxycarbonyl-1,8-diamino-3,6-dioxaoctane in Me2SO–NaH–KBr, respectively.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 132-133

Synthesis of novel chiral macrocyclic ligands bearing methyl 4,6-O-benzylidene-α-D-mannopyranoside

M. Pietraszkiewicz and J. J. ak, J. Chem. Soc., Chem. Commun., 1983, 132 DOI: 10.1039/C39830000132

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