Home / Publications / An efficient synthesis of symmetrical 2,5-diaryl-1,3,4-oxadiazoles

An efficient synthesis of symmetrical 2,5-diaryl-1,3,4-oxadiazoles

Sergei Igorevich Luiksaar 1
Sergei Igorevich Luiksaar
Leonid Isaakovich Belen'kii 1
Leonid Isaakovich Belen'kii
Mikhail Mikhailovich Krayushkin 1
Mikhail Mikhailovich Krayushkin
Published 1998-09-10
CommunicationVolume 8, Issue 4, 136-137
2
Share
Cite this
GOST
 | 
Cite this
GOST Copy
Luiksaar S. I., Belen'kii L. I., Krayushkin M. M. An efficient synthesis of symmetrical 2,5-diaryl-1,3,4-oxadiazoles // Mendeleev Communications. 1998. Vol. 8. No. 4. pp. 136-137.
GOST all authors (up to 50) Copy
Luiksaar S. I., Belen'kii L. I., Krayushkin M. M. An efficient synthesis of symmetrical 2,5-diaryl-1,3,4-oxadiazoles // Mendeleev Communications. 1998. Vol. 8. No. 4. pp. 136-137.
RIS
 | 
Cite this
RIS Copy
TY - JOUR
DO - 10.1070/MC1998v008n04ABEH000983
UR - https://mendcomm.colab.ws/publications/10.1070/MC1998v008n04ABEH000983
TI - An efficient synthesis of symmetrical 2,5-diaryl-1,3,4-oxadiazoles
T2 - Mendeleev Communications
AU - Luiksaar, Sergei Igorevich
AU - Belen'kii, Leonid Isaakovich
AU - Krayushkin, Mikhail Mikhailovich
PY - 1998
DA - 1998/09/10
PB - Mendeleev Communications
SP - 136-137
IS - 4
VL - 8
ER -
BibTex
 | 
Cite this
BibTex (up to 50 authors) Copy
@article{1998_Luiksaar,
author = {Sergei Igorevich Luiksaar and Leonid Isaakovich Belen'kii and Mikhail Mikhailovich Krayushkin},
title = {An efficient synthesis of symmetrical 2,5-diaryl-1,3,4-oxadiazoles},
journal = {Mendeleev Communications},
year = {1998},
volume = {8},
publisher = {Mendeleev Communications},
month = {Sep},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1998v008n04ABEH000983},
number = {4},
pages = {136--137},
doi = {10.1070/MC1998v008n04ABEH000983}
}
MLA
Cite this
MLA Copy
Luiksaar, Sergei Igorevich, et al. “An efficient synthesis of symmetrical 2,5-diaryl-1,3,4-oxadiazoles.” Mendeleev Communications, vol. 8, no. 4, Sep. 1998, pp. 136-137. https://mendcomm.colab.ws/publications/10.1070/MC1998v008n04ABEH000983.

Abstract

The interaction of trichloromethylarenes with excess hydrazine hydrate in alcohols leads to symmetrical 2,5-diaryl-1,3,4-oxadiazoles in 68–98% yields.

References

1.
10.1070/MC1998v008n04ABEH000983_bib1
Poddubnyi
Khim. Geterotsikl. Soedin., 1994
2.
10.1070/MC1998v008n04ABEH000983_bib2
Poddubnyi
Izv. Akad. Nauk, Ser. Khim., 1996
3.
10.1070/MC1998v008n04ABEH000983_bib3
Quemeneur
Compt. Rend. (C), 1971
4.
10.1070/MC1998v008n04ABEH000983_bib4
Quemeneur
Compt. Rend. (C), 1974
5.
10.1070/MC1998v008n04ABEH000983_bib5
Dvorko
Zh. Obshch. Khim., 1987
6.
THE PHOTO-INDUCED ALCOHOLYSIS OF BENZOTRICHLORIDE
Ishigami T., Kinoshita Y., Sugimori A.
Chemistry Letters, 1974
8.
Reaction of Phenyltrichloromethane with Semicarbazide and Thiosemicarbazide Derivatives
Sami Shawali A., M. Hassaneen H., H. Shetta A., M. Elwan N.
Heterocycles, 1982
9.
2,5-Diaryloxazoles and 2,5-Diaryl-1,3,4-oxadiazoles
Hayes F.N., Rogers B.S., Ott D.G.
Journal of the American Chemical Society, 1955
10.
10.1070/MC1998v008n04ABEH000983_bib10
Chiriac
Rev. Roum. Chim., 1987