Issue 1, 1995

Synthesis, conformational flexibility and preliminary complexation behaviour of α,α′-trehalose-based macrocycles containing thiourea spacers

Abstract

An efficient synthesis of macrocyclic ligands incorporating two α,α′-trehalose subunits linked through the primary C-6,6′ positions by means of 1,3-thiourea spacers is reported; the Z/E configuration of the N–C([double bond, length half m-dash]S) bonds is governed by intramolecular hydrogen bonding as well as steric factors.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 57-58

Synthesis, conformational flexibility and preliminary complexation behaviour of α,α′-trehalose-based macrocycles containing thiourea spacers

J. M. G. Fernández, J. L. J. Blanco, C. O. Mellet and J. Fuentes, J. Chem. Soc., Chem. Commun., 1995, 57 DOI: 10.1039/C39950000057

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