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Article Abstract
A preparative synthesis of previously unknown 21- and 14-membered azamacrocycles acid-promoted cyclotrimerization or cyclodimerization of three readily available precursors, namely, 1-amino-6-hydroxy-4,6-dimethylhexahydropyrimidine-2-thione, 4-(4-oxopent-2-yl)thiosemicarbazide hydrazone, and 5,7-dimethyl-1,4,5,6-tetrahydro-3-1,2,4-triazepine-3-thione has been developed. A dramatic dependence of the selectivity of macrocyclization on the reaction conditions is demonstrated. The thermodynamic aspects of the reactions are discussed based on experimental data and DFT calculation results. Plausible pathways for the formation of macrocycles are proposed.
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Article Synopsis
- - A new 14-membered cyclic compound containing amide, amino, and carbamate groups was accidentally discovered, resulting from the separation of larger cyclic compounds.
- - The structure of this new compound is unique because it includes a carbon monoxide insertion between specific positions in its ring structure, which was confirmed through a separate synthesis process.
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