Home / Publications / Selectivity of the Lewis acid-induced transformations of polyfunctional compounds containing a 4,6-dialkoxy-7-(arylthio)heptene moiety

Selectivity of the Lewis acid-induced transformations of polyfunctional compounds containing a 4,6-dialkoxy-7-(arylthio)heptene moiety

Dmitrii Sergeevich Chekmarev 1
Dmitrii Sergeevich Chekmarev
, 
Andrey V Maskaev 1
Andrey V Maskaev
, 
Georgy Valer'evich Zatonsky 2
Georgy Valer'evich Zatonsky
, 
Margarita Ivanovna Lazareva 1
Margarita Ivanovna Lazareva
, 
Ron Caple 3
Ron Caple
, 
William Arturovich Smit 2
William Arturovich Smit
10.1070/MC2001v011n05ABEH001513
Published 2001-10-23
Communication , Volume 11, Issue 5, 176-178
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Chekmarev D. S. et al. Selectivity of the Lewis acid-induced transformations of polyfunctional compounds containing a 4,6-dialkoxy-7-(arylthio)heptene moiety // Mendeleev Communications. 2001. Vol. 11. No. 5. pp. 176-178.
GOST all authors (up to 50) Copy
Chekmarev D. S., Maskaev A. V., Zatonsky G. V., Lazareva M. I., Caple R., Smit W. A. Selectivity of the Lewis acid-induced transformations of polyfunctional compounds containing a 4,6-dialkoxy-7-(arylthio)heptene moiety // Mendeleev Communications. 2001. Vol. 11. No. 5. pp. 176-178.
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TY - JOUR
DO - 10.1070/MC2001v011n05ABEH001513
UR - https://mendcomm.colab.ws/publications/10.1070/MC2001v011n05ABEH001513
TI - Selectivity of the Lewis acid-induced transformations of polyfunctional compounds containing a 4,6-dialkoxy-7-(arylthio)heptene moiety
T2 - Mendeleev Communications
AU - Chekmarev, Dmitrii Sergeevich
AU - Maskaev, Andrey V
AU - Zatonsky, Georgy Valer'evich
AU - Lazareva, Margarita Ivanovna
AU - Caple, Ron
AU - Smit, William Arturovich
PY - 2001
DA - 2001/10/23
PB - Mendeleev Communications
SP - 176-178
IS - 5
VL - 11
ER -
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@article{2001_Chekmarev,
author = {Dmitrii Sergeevich Chekmarev and Andrey V Maskaev and Georgy Valer'evich Zatonsky and Margarita Ivanovna Lazareva and Ron Caple and William Arturovich Smit},
title = {Selectivity of the Lewis acid-induced transformations of polyfunctional compounds containing a 4,6-dialkoxy-7-(arylthio)heptene moiety},
journal = {Mendeleev Communications},
year = {2001},
volume = {11},
publisher = {Mendeleev Communications},
month = {Oct},
url = {https://mendcomm.colab.ws/publications/10.1070/MC2001v011n05ABEH001513},
number = {5},
pages = {176--178},
doi = {10.1070/MC2001v011n05ABEH001513}
}
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Chekmarev, Dmitrii Sergeevich, et al. “Selectivity of the Lewis acid-induced transformations of polyfunctional compounds containing a 4,6-dialkoxy-7-(arylthio)heptene moiety.” Mendeleev Communications, vol. 11, no. 5, Oct. 2001, pp. 176-178. https://mendcomm.colab.ws/publications/10.1070/MC2001v011n05ABEH001513.

Abstract

The interaction of the title adducts with Lewis acids may proceed as an attack at either β-alkoxy or δ-alkoxy group to the arylthio substituent leading to the formation of substituted cyclohexane or 1,3-diene derivatives, respectively.

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