Vicarious nucleophilic substitution of hydrogen in nitrophenyl toluenesulfonates
Publication type: Journal Article
Publication date: 1997-03-01
scimago Q3
wos Q2
SJR: 0.426
CiteScore: 4.1
Impact factor: 2.2
ISSN: 00404020, 14645416
Organic Chemistry
Drug Discovery
Biochemistry
Abstract
Toluenesulfonates of nitrophenols react with carbanions possessing leaving groups giving products of the vicarious nucleophilic substitution of hydrogen. The yields and orientation depend on the reaction conditions and the structure of the reagents. The products obtained can be easily hydrolyzed to the corresponding phenols or — in certain cases — to hydroxynitrobenzaldehydes.
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Makosza M. et al. Vicarious nucleophilic substitution of hydrogen in nitrophenyl toluenesulfonates // Tetrahedron. 1997. Vol. 53. No. 13. pp. 4739-4750.
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Mąkosza M., Ziobrowski T., Serebriakov M., Kwast A. Vicarious nucleophilic substitution of hydrogen in nitrophenyl toluenesulfonates // Tetrahedron. 1997. Vol. 53. No. 13. pp. 4739-4750.
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TY - JOUR
DO - 10.1016/S0040-4020(97)00143-9
UR - https://doi.org/10.1016/S0040-4020(97)00143-9
TI - Vicarious nucleophilic substitution of hydrogen in nitrophenyl toluenesulfonates
T2 - Tetrahedron
AU - Mąkosza, Mieczysław
AU - Ziobrowski, Tadeusz
AU - Serebriakov, Mikhail
AU - Kwast, Andrzej
PY - 1997
DA - 1997/03/01
PB - Elsevier
SP - 4739-4750
IS - 13
VL - 53
SN - 0040-4020
SN - 1464-5416
ER -
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BibTex (up to 50 authors)
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@article{1997_Makosza,
author = {Mieczysław Mąkosza and Tadeusz Ziobrowski and Mikhail Serebriakov and Andrzej Kwast},
title = {Vicarious nucleophilic substitution of hydrogen in nitrophenyl toluenesulfonates},
journal = {Tetrahedron},
year = {1997},
volume = {53},
publisher = {Elsevier},
month = {mar},
url = {https://doi.org/10.1016/S0040-4020(97)00143-9},
number = {13},
pages = {4739--4750},
doi = {10.1016/S0040-4020(97)00143-9}
}
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MLA
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Makosza, Mieczysław, et al. “Vicarious nucleophilic substitution of hydrogen in nitrophenyl toluenesulfonates.” Tetrahedron, vol. 53, no. 13, Mar. 1997, pp. 4739-4750. https://doi.org/10.1016/S0040-4020(97)00143-9.