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The reaction of chloroalkyl(vinyl)silanes with N,N-dichloro sulfonamides

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Ushakova I. V., Shainyan B. A. The reaction of chloroalkyl(vinyl)silanes with N,N-dichloro sulfonamides // Mendeleev Communications. 2020. Vol. 30. No. 6. pp. 794-795.
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Ushakova I. V., Shainyan B. A. The reaction of chloroalkyl(vinyl)silanes with N,N-dichloro sulfonamides // Mendeleev Communications. 2020. Vol. 30. No. 6. pp. 794-795.
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TY - JOUR
DO - 10.1016/j.mencom.2020.11.035
UR - https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.11.035
TI - The reaction of chloroalkyl(vinyl)silanes with N,N-dichloro sulfonamides
T2 - Mendeleev Communications
AU - Ushakova, Irina Vladimirovna
AU - Shainyan, Bagrat Armenovich
PY - 2020
DA - 2020/11/03
PB - Mendeleev Communications
SP - 794-795
IS - 6
VL - 30
ER -
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@article{2020_Ushakova,
author = {Irina Vladimirovna Ushakova and Bagrat Armenovich Shainyan},
title = {The reaction of chloroalkyl(vinyl)silanes with N,N-dichloro sulfonamides},
journal = {Mendeleev Communications},
year = {2020},
volume = {30},
publisher = {Mendeleev Communications},
month = {Nov},
url = {https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.11.035},
number = {6},
pages = {794--795},
doi = {10.1016/j.mencom.2020.11.035}
}
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Ushakova, Irina Vladimirovna, and Bagrat Armenovich Shainyan. “The reaction of chloroalkyl(vinyl)silanes with N,N-dichloro sulfonamides.” Mendeleev Communications, vol. 30, no. 6, Nov. 2020, pp. 794-795. https://mendcomm.colab.ws/publications/10.1016/j.mencom.2020.11.035.

Keywords

N,N-dichloro sulfonamides
1,3-azasilolidines
chloroalkyl(dimethyl)vinylsilanes
chloroamidation
heterocyclization

Abstract

The reactions of N,N-dichloroarenesulfonamides with chloromethyl(dimethyl)vinylsilane or of N,N-dichlorotrifluoromethanesulfonamide with chloropropyl(dimethyl)vinylsilanegive the NH- and NCl-containing products of chlorosulfonamidation of the double bonds. In contrast, N,N-(dichloro)trifluoromethanesulfonamide reacts with chloromethyl(dimethyl)vinylsilane to afford 4-chloro-3,3-dimethyl1-[(trifluoroethyl) sulfonyl]-1,3-azasilolidine via intramolecular heterocyclization.

References

4.
Oxidative sulfamidation of vinyl silanes: A route to diverse silylated N-Heterocycles
Astakhova V.V., Shainyan B.A., Moskalik M.Y., Sterkhova I.V.
Tetrahedron, 2019
5.
Ushakova I.V., Shainyan B.A.
Mendeleev Communications, 2020
6.
Drug design based on the carbon/silicon switch strategy
Lazareva N.F., Lazarev I.M.
Russian Chemical Bulletin, 2015
7.
Progress in the medicinal chemistry of silicon: C/Si exchange and beyond
8.
Heterocyclization and solvent interception upon oxidative triflamidation of allyl ethers, amines and silanes
Ganin A.S., Moskalik M.Y., Astakhova V.V., Sterkhova I.V., Shainyan B.A.
Tetrahedron, 2020
9.
10.1016/j.mencom.2020.11.035_bib0045
Nazaretyan
Zh. Org. Khim., 1974
10.
Electrophilic Cyclization of Dimethyl(ω-phenylaminoalkyl)alkenylsilanes
Kirpichenko S.V., Abrosimova A.T., Albanov A.I., Voronkov M.G.
Russian Journal of General Chemistry, 2001