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Thienopentathiepins and pentathiepinofuran

Stanislav Anatol'evich Amelichev 1
Stanislav Anatol'evich Amelichev
, 
Lidia Sergeevna Konstantinova 1
Lidia Sergeevna Konstantinova
, 
Oleg Alexeevich Rakitin 1
Oleg Alexeevich Rakitin
, 
Charles W Rees 2
Charles W Rees
10.1070/MC2006v016n06ABEH002454
Published 2006-12-06
Communication , Volume 16, Issue 6, 289-290
7
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Amelichev S. A. et al. Thienopentathiepins and pentathiepinofuran // Mendeleev Communications. 2006. Vol. 16. No. 6. pp. 289-290.
GOST all authors (up to 50) Copy
Amelichev S. A., Konstantinova L. S., Rakitin O. A., Rees C. W. Thienopentathiepins and pentathiepinofuran // Mendeleev Communications. 2006. Vol. 16. No. 6. pp. 289-290.
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TY - JOUR
DO - 10.1070/MC2006v016n06ABEH002454
UR - https://mendcomm.colab.ws/publications/10.1070/MC2006v016n06ABEH002454
TI - Thienopentathiepins and pentathiepinofuran
T2 - Mendeleev Communications
AU - Amelichev, Stanislav Anatol'evich
AU - Konstantinova, Lidia Sergeevna
AU - Rakitin, Oleg Alexeevich
AU - Rees, Charles W
PY - 2006
DA - 2006/12/06
PB - Mendeleev Communications
SP - 289-290
IS - 6
VL - 16
ER -
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@article{2006_Amelichev,
author = {Stanislav Anatol'evich Amelichev and Lidia Sergeevna Konstantinova and Oleg Alexeevich Rakitin and Charles W Rees},
title = {Thienopentathiepins and pentathiepinofuran},
journal = {Mendeleev Communications},
year = {2006},
volume = {16},
publisher = {Mendeleev Communications},
month = {Dec},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2006v016n06ABEH002454},
number = {6},
pages = {289--290},
doi = {10.1070/MC2006v016n06ABEH002454}
}
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Amelichev, Stanislav Anatol'evich, et al. “Thienopentathiepins and pentathiepinofuran.” Mendeleev Communications, vol. 16, no. 6, Dec. 2006, pp. 289-290. https://mendcomm.colab.ws/publications/10.1070/MC2006v016n06ABEH002454.

Abstract

Thienopentathiepins and pentathiepinofuran were synthesised by the reaction of thiophenes and 2,5-dimethylfuran with S2Cl2 and N-ethyldiisopropylamine in chloroform at low temperature; thienopentathiepin 2 reacts with methyl propiolate and triphenylphosphine to give a pair of regioisomers.

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