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Synthesis of new sulfinyl derivatives of 4,​5-​diphenyl-​4H-​1,​2,​4-​triazoles. / Rodygin, K. S.; Rubtsova, S. A.; Kuchin, A. V.

In: Russian Journal of Organic Chemistry, Vol. 47, No. 9, 2011, p. 1433-1435.

Research output: Contribution to journalArticle

Harvard

Rodygin, KS, Rubtsova, SA & Kuchin, AV 2011, 'Synthesis of new sulfinyl derivatives of 4,​5-​diphenyl-​4H-​1,​2,​4-​triazoles', Russian Journal of Organic Chemistry, vol. 47, no. 9, pp. 1433-1435. https://doi.org/10.1134/S1070428011090302

APA

Rodygin, K. S., Rubtsova, S. A., & Kuchin, A. V. (2011). Synthesis of new sulfinyl derivatives of 4,​5-​diphenyl-​4H-​1,​2,​4-​triazoles. Russian Journal of Organic Chemistry, 47(9), 1433-1435. https://doi.org/10.1134/S1070428011090302

Vancouver

Author

Rodygin, K. S. ; Rubtsova, S. A. ; Kuchin, A. V. / Synthesis of new sulfinyl derivatives of 4,​5-​diphenyl-​4H-​1,​2,​4-​triazoles. In: Russian Journal of Organic Chemistry. 2011 ; Vol. 47, No. 9. pp. 1433-1435.

BibTeX

@article{a3618acc446e41219f269f21c73c1360,
title = "Synthesis of new sulfinyl derivatives of 4,​5-​diphenyl-​4H-​1,​2,​4-​triazoles",
abstract = "The alkylation of 4,​5-​diphenyl-​4H-​1,​2,​4-​triazole-​3-​thiol with alkyl iodides in alc. alkali led to 3-​alkylsulfanyl-​4,​5-​diphenyl-​4H-​1,​2,​4-​triazoles in quant. yields. The asym. oxidn. of alkylsulfanyl derivs. by the using Kagan's reagent and cumyl hydroperoxide as oxidant gave the desired compds., 3-​alkylsulfinyl-​4,​5-​diphenyl-​4H-​1,​2,​4-​triazoles.",
author = "Rodygin, {K. S.} and Rubtsova, {S. A.} and Kuchin, {A. V.}",
year = "2011",
doi = "10.1134/S1070428011090302",
language = "не определен",
volume = "47",
pages = "1433--1435",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "9",

}

RIS

TY - JOUR

T1 - Synthesis of new sulfinyl derivatives of 4,​5-​diphenyl-​4H-​1,​2,​4-​triazoles

AU - Rodygin, K. S.

AU - Rubtsova, S. A.

AU - Kuchin, A. V.

PY - 2011

Y1 - 2011

N2 - The alkylation of 4,​5-​diphenyl-​4H-​1,​2,​4-​triazole-​3-​thiol with alkyl iodides in alc. alkali led to 3-​alkylsulfanyl-​4,​5-​diphenyl-​4H-​1,​2,​4-​triazoles in quant. yields. The asym. oxidn. of alkylsulfanyl derivs. by the using Kagan's reagent and cumyl hydroperoxide as oxidant gave the desired compds., 3-​alkylsulfinyl-​4,​5-​diphenyl-​4H-​1,​2,​4-​triazoles.

AB - The alkylation of 4,​5-​diphenyl-​4H-​1,​2,​4-​triazole-​3-​thiol with alkyl iodides in alc. alkali led to 3-​alkylsulfanyl-​4,​5-​diphenyl-​4H-​1,​2,​4-​triazoles in quant. yields. The asym. oxidn. of alkylsulfanyl derivs. by the using Kagan's reagent and cumyl hydroperoxide as oxidant gave the desired compds., 3-​alkylsulfinyl-​4,​5-​diphenyl-​4H-​1,​2,​4-​triazoles.

U2 - 10.1134/S1070428011090302

DO - 10.1134/S1070428011090302

M3 - статья

VL - 47

SP - 1433

EP - 1435

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 9

ER -

ID: 5551784