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Adducts of ArSCl with vinyl ethers or esters as synthones in geminal alkylation

William Arturovich Smit 1
William Arturovich Smit
, 
Alexei V Gromov 2
Alexei V Gromov
, 
Elisey Alekseevich Yagodkin 1
Elisey Alekseevich Yagodkin
10.1070/MC2003v013n01ABEH001710
Published 2003-03-04
Communication , Volume 13, Issue 1, 21-23
4
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Smit W. A., Gromov A. V., Yagodkin E. A. Adducts of ArSCl with vinyl ethers or esters as synthones in geminal alkylation // Mendeleev Communications. 2003. Vol. 13. No. 1. pp. 21-23.
GOST all authors (up to 50) Copy
Smit W. A., Gromov A. V., Yagodkin E. A. Adducts of ArSCl with vinyl ethers or esters as synthones in geminal alkylation // Mendeleev Communications. 2003. Vol. 13. No. 1. pp. 21-23.
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TY - JOUR
DO - 10.1070/MC2003v013n01ABEH001710
UR - https://mendcomm.colab.ws/publications/10.1070/MC2003v013n01ABEH001710
TI - Adducts of ArSCl with vinyl ethers or esters as synthones in geminal alkylation
T2 - Mendeleev Communications
AU - Smit, William Arturovich
AU - Gromov, Alexei V
AU - Yagodkin, Elisey Alekseevich
PY - 2003
DA - 2003/03/04
PB - Mendeleev Communications
SP - 21-23
IS - 1
VL - 13
ER -
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@article{2003_Smit,
author = {William Arturovich Smit and Alexei V Gromov and Elisey Alekseevich Yagodkin},
title = {Adducts of ArSCl with vinyl ethers or esters as synthones in geminal alkylation},
journal = {Mendeleev Communications},
year = {2003},
volume = {13},
publisher = {Mendeleev Communications},
month = {Mar},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2003v013n01ABEH001710},
number = {1},
pages = {21--23},
doi = {10.1070/MC2003v013n01ABEH001710}
}
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Smit, William Arturovich, et al. “Adducts of ArSCl with vinyl ethers or esters as synthones in geminal alkylation.” Mendeleev Communications, vol. 13, no. 1, Mar. 2003, pp. 21-23. https://mendcomm.colab.ws/publications/10.1070/MC2003v013n01ABEH001710.

Abstract

The in situ-prepared adducts of arylsulfenyl chloride and vinyl ethers (esters) were employed as synthetic equivalents of 1,1-bis-electrophiles in the Lewis acid-promoted reaction sequence with two different carbon nucleophiles resulting in the formation of geminal bisalkylation products.

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