Answers are grounded in this paper and cite their sources.
A number of 2‐hydroxycycloalkyl‐substituted 1,3,4‐oxadiazole, 1,3,4‐thiadiazole and 1,2,4‐triazole derivatives were prepared by different methods from cis‐ and trans‐2‐hydroxy‐1‐cycloalkanecarbohydrazides and their isocyanate or isothiocyanate adducts. In contrast with the related ring‐closure reactions of 2‐aminobenzoylhydrazides, no condensed skeleton heterocycles were formed in this case.
No takes yet. Share an insight, caveat, or question.
Fülöp et al. (1990) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: