Issue 18, 2001

1,2,4,3,5-Benzotrithiadiazepine and its unexpected hydrolysis to unusual 7H,14H-dibenzo[d,i][1,2,6,7,3,8]tetrathiadiazecine

Abstract

Previously unknown 1,2,4,3,5-benzotrithiadiazepine 1 was prepared by 1∶1 condensation of Ph-N[double bond, length half m-dash]S[double bond, length half m-dash]N-SiMe3 with S2Cl2 followed by intramolecular ortho-cyclization of [Ph-N[double bond, length half m-dash]S[double bond, length half m-dash]N-S-S-Cl] intermediate, and hydrolyzed in pyridine to unusual macrocyclic 7H,14H-dibenzo[d,i][1,2,6,7,3,8]tetrathiadiazecine 2.

Supplementary files

Article information

Article type
Communication
Submitted
06 Jun 2001
Accepted
02 Aug 2001
First published
03 Sep 2001

Chem. Commun., 2001, 1774-1775

1,2,4,3,5-Benzotrithiadiazepine and its unexpected hydrolysis to unusual 7H,14H-dibenzo[d,i][1,2,6,7,3,8]tetrathiadiazecine

A. Yu. Makarov, M. M. Shakirov, K. V. Shuvaev, I. Yu. Bagryanskaya, Y. V. Gatilov and A. V. Zibarev, Chem. Commun., 2001, 1774 DOI: 10.1039/B105001J

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