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Short Note

6,10-Dichloro-1-oxa-4,8-dithia-7,9-diazaspiro[4.5]deca-6,9-diene

1
Department of Life Sciences, School of Sciences, European University Cyprus, 6 Diogenis Str., Engomi, P.O. Box 22006, Nicosia 1516, Cyprus
2
Department of Chemistry, University of Cyprus, P.O. Box 20537, Nicosia 1678, Cyprus
*
Author to whom correspondence should be addressed.
Academic Editor: R. Alan Aitken
Molbank 2022, 2022(2), M1377; https://doi.org/10.3390/M1377
Received: 12 May 2022 / Revised: 1 June 2022 / Accepted: 2 June 2022 / Published: 3 June 2022
(This article belongs to the Section Organic Synthesis)
Reaction of 3,4,4,5-tetrachloro-4H-1,2,6-thiadiazine with 2-mercaptoethan-1-ol (1 equiv.) gave 6,10-dichloro-1-oxa-4,8-dithia-7,9-diazaspiro[4.5]deca-6,9-diene in 12% yield. The compound was fully characterized. View Full-Text
Keywords: heterocycle; 1,2,6-thiadiazine; spirocycle; oxathiolane heterocycle; 1,2,6-thiadiazine; spirocycle; oxathiolane
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MDPI and ACS Style

Kalogirou, A.S.; Koutentis, P.A. 6,10-Dichloro-1-oxa-4,8-dithia-7,9-diazaspiro[4.5]deca-6,9-diene. Molbank 2022, 2022, M1377. https://doi.org/10.3390/M1377

AMA Style

Kalogirou AS, Koutentis PA. 6,10-Dichloro-1-oxa-4,8-dithia-7,9-diazaspiro[4.5]deca-6,9-diene. Molbank. 2022; 2022(2):M1377. https://doi.org/10.3390/M1377

Chicago/Turabian Style

Kalogirou, Andreas S., and Panayiotis A. Koutentis. 2022. "6,10-Dichloro-1-oxa-4,8-dithia-7,9-diazaspiro[4.5]deca-6,9-diene" Molbank 2022, no. 2: M1377. https://doi.org/10.3390/M1377

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