Synthesis of 2,5-Disubstituted 1,3,4-Oxadiazoles and Their Precursors

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Title:Synthesis of 2,5-Disubstituted 1,3,4-Oxadiazoles and Their Precursors
Creators:
Jedlovská, Eva
Gavláková, Edita
Journal or Publication Title:
Collection of Czechoslovak Chemical Communications, 59, 8, pp. 1892-1896

Abstract

<p>The characteristic feature of many commercial agrochemicals and drugs is the 5-nitro-2-furyl or 2,5-dimethyl-3-furyl building block. Within the scope of our research aimed at utilization of dipolar cycloaddition reactions to prepare new compounds with potential biological and phytoeffectorial activity, we report on the synthesis of some substituted hydrazones <i>I</i> and their intramolecular cycloaddition to 2,5-disubstituted 1,3,4-oxadiazoles <i>II</i>. The basic IR, <sup>1</sup>H NMR as well as mass spectral data of final products are presented.

Title:Synthesis of 2,5-Disubstituted 1,3,4-Oxadiazoles and Their Precursors
Creators:
Jedlovská, Eva
Gavláková, Edita
Divisions:Life and Chemical Sciences > Institute of Organic Chemistry and Biochemistry > Collection of Czechoslovak Chemical Communications
Journal or Publication Title:Collection of Czechoslovak Chemical Communications
Volume:59
Number:8
Page Range:pp. 1892-1896
ISSN:0010-0765
E-ISSN:1212-6950
Publisher:Institute of Organic Chemistry and Biochemistry
Related URLs:
URLURL Type
http://dx.doi.org/10.1135/cccc19941892UNSPECIFIED
ID Code:614
Item Type:Article
Deposited On:06 Feb 2009 17:02
Last Modified:06 Feb 2009 16:02

Citation

Jedlovská, Eva; Gavláková, Edita (1994) Synthesis of 2,5-Disubstituted 1,3,4-Oxadiazoles and Their Precursors. Collection of Czechoslovak Chemical Communications, 59 (8). pp. 1892-1896. ISSN 0010-0765

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