Synthesis of new macrocycles. Part 5. Cyclization of 2,2′-dithiodibenzoic acid derivatives

Abstract
Condensation of 2,2′-dithiodibenzoyl chloride with a series of alkanediols, but-2-yne-1,4-diol, triethylene glycol, and tetraethylene glycol affords cyclic esters in yields ranging from 5 to 95%. On the basis of n.m.r. evidence, predictions are made regarding conformations of the macrocycles.

This publication has 0 references indexed in Scilit: