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Solvent-Free Synthesis of 2-[(Di)aminophenyl]-1,3,4-oxadiazoles. / Krinochkin, A. P.; Shtaitz, Ya. K.; Savchuk, M. I. et al.
In: Russian Journal of Organic Chemistry, Vol. 58, No. 7, 01.07.2022, p. 1064-1066.

Research output: Contribution to journal › Article › peer-review

Harvard

Krinochkin, AP, Shtaitz, YK, Savchuk, MI, Kopchuk, DS, Slovesnova, NV, Kovalev, IS, Nosova, EV, Zyryanov, GV & Chupakhin, ON 2022, 'Solvent-Free Synthesis of 2-[(Di)aminophenyl]-1,3,4-oxadiazoles', Russian Journal of Organic Chemistry, vol. 58, no. 7, pp. 1064-1066. https://doi.org/10.1134/S1070428022070181

APA

Krinochkin, A. P., Shtaitz, Y. K., Savchuk, M. I., Kopchuk, D. S., Slovesnova, N. V., Kovalev, I. S., Nosova, E. V., Zyryanov, G. V., & Chupakhin, O. N. (2022). Solvent-Free Synthesis of 2-[(Di)aminophenyl]-1,3,4-oxadiazoles. Russian Journal of Organic Chemistry, 58(7), 1064-1066. https://doi.org/10.1134/S1070428022070181

Vancouver

Krinochkin AP, Shtaitz YK, Savchuk MI, Kopchuk DS, Slovesnova NV, Kovalev IS et al. Solvent-Free Synthesis of 2-[(Di)aminophenyl]-1,3,4-oxadiazoles. Russian Journal of Organic Chemistry. 2022 Jul 1;58(7):1064-1066. doi: 10.1134/S1070428022070181

Author

Krinochkin, A. P. ; Shtaitz, Ya. K. ; Savchuk, M. I. et al. / Solvent-Free Synthesis of 2-[(Di)aminophenyl]-1,3,4-oxadiazoles. In: Russian Journal of Organic Chemistry. 2022 ; Vol. 58, No. 7. pp. 1064-1066.

BibTeX

@article{ad57badbe68a4eb79095650fad9c12ee,
title = "Solvent-Free Synthesis of 2-[(Di)aminophenyl]-1,3,4-oxadiazoles",
abstract = "An efficient procedure has been developed for the synthesis of 2-phenyl-1,3,4-oxadiazole deriva­tives with one or two pyrrolidin-1-yl substituents in the benzene ring via nucleophilic substitution of fluorine in 2-[(di)fluorophenyl]-1,3,4-oxadiazole on heating with pyrrolidine under solvent-free conditions.",
keywords = "1,3,4-oxadiazoles, nucleophilic substitution of fluorine, pyrrolidine, solvent-free reactions",
author = "Krinochkin, {A. P.} and Shtaitz, {Ya. K.} and Savchuk, {M. I.} and Kopchuk, {D. S.} and Slovesnova, {N. V.} and Kovalev, {I. S.} and Nosova, {E. V.} and Zyryanov, {G. V.} and Chupakhin, {O. N.}",
year = "2022",
month = jul,
day = "1",
doi = "10.1134/S1070428022070181",
language = "English",
volume = "58",
pages = "1064--1066",
journal = "Russian Journal of Organic Chemistry",
issn = "1070-4280",
publisher = "Maik Nauka-Interperiodica Publishing",
number = "7",

}

RIS

TY - JOUR

T1 - Solvent-Free Synthesis of 2-[(Di)aminophenyl]-1,3,4-oxadiazoles

AU - Krinochkin, A. P.

AU - Shtaitz, Ya. K.

AU - Savchuk, M. I.

AU - Kopchuk, D. S.

AU - Slovesnova, N. V.

AU - Kovalev, I. S.

AU - Nosova, E. V.

AU - Zyryanov, G. V.

AU - Chupakhin, O. N.

PY - 2022/7/1

Y1 - 2022/7/1

N2 - An efficient procedure has been developed for the synthesis of 2-phenyl-1,3,4-oxadiazole deriva­tives with one or two pyrrolidin-1-yl substituents in the benzene ring via nucleophilic substitution of fluorine in 2-[(di)fluorophenyl]-1,3,4-oxadiazole on heating with pyrrolidine under solvent-free conditions.

AB - An efficient procedure has been developed for the synthesis of 2-phenyl-1,3,4-oxadiazole deriva­tives with one or two pyrrolidin-1-yl substituents in the benzene ring via nucleophilic substitution of fluorine in 2-[(di)fluorophenyl]-1,3,4-oxadiazole on heating with pyrrolidine under solvent-free conditions.

KW - 1,3,4-oxadiazoles

KW - nucleophilic substitution of fluorine

KW - pyrrolidine

KW - solvent-free reactions

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000854513500018

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85138202647

U2 - 10.1134/S1070428022070181

DO - 10.1134/S1070428022070181

M3 - Article

VL - 58

SP - 1064

EP - 1066

JO - Russian Journal of Organic Chemistry

JF - Russian Journal of Organic Chemistry

SN - 1070-4280

IS - 7

ER -

ID: 30949857