Orientation and mechanism of reactions of aromatic amines with sulfur monochloride
Тип публикации: Journal Article
Дата публикации: 1970-03-01
scimago Q4
wos Q4
БС3
SJR: 0.243
CiteScore: 2.7
Impact factor: 1
ISSN: 00093122, 15738353
Organic Chemistry
Краткое описание
The reaction of m-substituted anilines with sulfur monochloride has been studied. It has been shown that cyclization with the formation of 1, 3, 2-benzothiazathiolium compounds takes place in the position para to the substituent. The introduction of methoxy groups into o-nitroanilines interferes with the displacement of the nitro group by the chlorine atom. A nucleophilic reaction mechanism has been proposed according to which the nitro group is displaced after the formation of the thiathioniaazine ring.
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Strelets B. Kh. et al. Orientation and mechanism of reactions of aromatic amines with sulfur monochloride // Chemistry of Heterocyclic Compounds. 1970. Vol. 6. No. 3. pp. 327-329.
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Strelets B. Kh., Fros L. S., Todres Z. V. Orientation and mechanism of reactions of aromatic amines with sulfur monochloride // Chemistry of Heterocyclic Compounds. 1970. Vol. 6. No. 3. pp. 327-329.
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TY - JOUR
DO - 10.1007/bf00471234
UR - https://doi.org/10.1007/bf00471234
TI - Orientation and mechanism of reactions of aromatic amines with sulfur monochloride
T2 - Chemistry of Heterocyclic Compounds
AU - Strelets, B Kh
AU - Fros, L S
AU - Todres, Z. V.
PY - 1970
DA - 1970/03/01
PB - Springer Nature
SP - 327-329
IS - 3
VL - 6
SN - 0009-3122
SN - 1573-8353
ER -
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@article{1970_Strelets,
author = {B Kh Strelets and L S Fros and Z. V. Todres},
title = {Orientation and mechanism of reactions of aromatic amines with sulfur monochloride},
journal = {Chemistry of Heterocyclic Compounds},
year = {1970},
volume = {6},
publisher = {Springer Nature},
month = {mar},
url = {https://doi.org/10.1007/bf00471234},
number = {3},
pages = {327--329},
doi = {10.1007/bf00471234}
}
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MLA
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Strelets, B. Kh., et al. “Orientation and mechanism of reactions of aromatic amines with sulfur monochloride.” Chemistry of Heterocyclic Compounds, vol. 6, no. 3, Mar. 1970, pp. 327-329. https://doi.org/10.1007/bf00471234.