An Efficient Synthesis of New 2-Aryl-5-phenylazenyl-1,3,4-oxadiazole Derivatives from N, N' -Diarylcarbonohydrazides

Anna Kedzia; Karolina Jasiak; Agnieszka Kudelko

doi:10.1055/s-0037-1610105

An Efficient Synthesis of New 2-Aryl-5-phenylazenyl-1,3,4-oxadiazole Derivatives from N, N' -Diarylcarbonohydrazides

Anna Kedzia
, Karolina Jasiak
, Agnieszka Kudelko

Department of Chemical Organic Technology and Petrochemistry (RCH/RCH5)

Silesian University of Technology

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

7 Citations (Scopus)

Abstract

A series of new 1,3,4-oxadiazoles conjugated to aromatic substituents by an azo linker was synthesized in a four-step reaction sequence, involving cyclodehydration of a N, N' -diacylhydrazine fragment and dehydrogenation of the neighboring hydrazine fragment of the intermediate N, N' -diarylcarbonohydrazide.

Original language	English
Pages (from-to)	1745-1748
Number of pages	4
Journal	Synlett
Volume	29
Issue number	13
DOIs	https://doi.org/10.1055/s-0037-1610105
Publication status	Published - 19 Jun 2018

Keywords

1,3,4-oxadiazoles
azo compounds
cyclodehydration
dehydrogenation
heterocycles

ASJC Scopus subject areas

Organic Chemistry

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10.1055/s-0037-1610105

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abstract = "A series of new 1,3,4-oxadiazoles conjugated to aromatic substituents by an azo linker was synthesized in a four-step reaction sequence, involving cyclodehydration of a N, N' -diacylhydrazine fragment and dehydrogenation of the neighboring hydrazine fragment of the intermediate N, N' -diarylcarbonohydrazide.",

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AU - Jasiak, Karolina

AU - Kudelko, Agnieszka

PY - 2018/6/19

Y1 - 2018/6/19

N2 - A series of new 1,3,4-oxadiazoles conjugated to aromatic substituents by an azo linker was synthesized in a four-step reaction sequence, involving cyclodehydration of a N, N' -diacylhydrazine fragment and dehydrogenation of the neighboring hydrazine fragment of the intermediate N, N' -diarylcarbonohydrazide.

AB - A series of new 1,3,4-oxadiazoles conjugated to aromatic substituents by an azo linker was synthesized in a four-step reaction sequence, involving cyclodehydration of a N, N' -diacylhydrazine fragment and dehydrogenation of the neighboring hydrazine fragment of the intermediate N, N' -diarylcarbonohydrazide.

KW - 1,3,4-oxadiazoles

KW - azo compounds

KW - cyclodehydration

KW - dehydrogenation

KW - heterocycles

UR - https://www.scopus.com/pages/publications/85048853325

U2 - 10.1055/s-0037-1610105

DO - 10.1055/s-0037-1610105

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ER -

An Efficient Synthesis of New 2-Aryl-5-phenylazenyl-1,3,4-oxadiazole Derivatives from N, N' -Diarylcarbonohydrazides

Abstract

Keywords

ASJC Scopus subject areas

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