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New routes to 1,2-dithiole-3-thiones and 3-imines

Vladimir Anatol'evich Ogurtsov 1
Vladimir Anatol'evich Ogurtsov
, 
Oleg Alexeevich Rakitin 1
Oleg Alexeevich Rakitin
, 
Charles W Rees 2
Charles W Rees
, 
Alexey Aleksandrovich Smolentsev 1
Alexey Aleksandrovich Smolentsev
, 
Konstantin Alexandrovich Lyssenko 3
Konstantin Alexandrovich Lyssenko
10.1070/MC2005v015n01ABEH002057
Published 2005-02-09
Communication , Volume 15, Issue 1, 20-21
6
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Ogurtsov V. A. et al. New routes to 1,2-dithiole-3-thiones and 3-imines // Mendeleev Communications. 2005. Vol. 15. No. 1. pp. 20-21.
GOST all authors (up to 50) Copy
Ogurtsov V. A., Rakitin O. A., Rees C. W., Smolentsev A. A., Lyssenko K. A. New routes to 1,2-dithiole-3-thiones and 3-imines // Mendeleev Communications. 2005. Vol. 15. No. 1. pp. 20-21.
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TY - JOUR
DO - 10.1070/MC2005v015n01ABEH002057
UR - https://mendcomm.colab.ws/publications/10.1070/MC2005v015n01ABEH002057
TI - New routes to 1,2-dithiole-3-thiones and 3-imines
T2 - Mendeleev Communications
AU - Ogurtsov, Vladimir Anatol'evich
AU - Rakitin, Oleg Alexeevich
AU - Rees, Charles W
AU - Smolentsev, Alexey Aleksandrovich
AU - Lyssenko, Konstantin Alexandrovich
PY - 2005
DA - 2005/02/09
PB - Mendeleev Communications
SP - 20-21
IS - 1
VL - 15
ER -
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@article{2005_Ogurtsov,
author = {Vladimir Anatol'evich Ogurtsov and Oleg Alexeevich Rakitin and Charles W Rees and Alexey Aleksandrovich Smolentsev and Konstantin Alexandrovich Lyssenko},
title = {New routes to 1,2-dithiole-3-thiones and 3-imines},
journal = {Mendeleev Communications},
year = {2005},
volume = {15},
publisher = {Mendeleev Communications},
month = {Feb},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2005v015n01ABEH002057},
number = {1},
pages = {20--21},
doi = {10.1070/MC2005v015n01ABEH002057}
}
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Ogurtsov, Vladimir Anatol'evich, et al. “New routes to 1,2-dithiole-3-thiones and 3-imines.” Mendeleev Communications, vol. 15, no. 1, Feb. 2005, pp. 20-21. https://mendcomm.colab.ws/publications/10.1070/MC2005v015n01ABEH002057.

Abstract

The reaction of readily available 3,4,5-trichloro-1,2-dithiolium chloride 1 and 4,5-dichloro-1,2-dithiole-3-thione 2 with o-substituted anilines provides a simple route to 1,2-dithiole-3-thiones and 3-imines, which can be cyclised to give new, more complex heterocyclic systems such as 1,2-dithiolo[4,3-b][1,4]benzoxazine of potential value in cancer chemotherapy

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