Results 161 to 170 of about 4,245 (200)

Low Sensitivity Energetic Material Based on 1,2,4-Oxadiazole

open access: yesFirePhysChem
Gan Jin   +4 more
openaire   +1 more source

Bioisosterism: 1,2,4‐Oxadiazole Rings

ChemMedChem, 2023
AbstractAlthough studies in drug discovery have gained momentum in recent years, the conversion of drugs in use today into less toxic derivatives with pharmacologically superior properties is still of great importance in drug research. Bioisosterism facilitates the conversion of drugs into derivatives that present more positive pharmacological and ...
Merve Camci, Nilgün Karali
openaire   +2 more sources

Banana-shaped 1,2,4-oxadiazoles

Pramana, 2003
3,5-Disubstituted 1,2,4-oxadiazoles are a new type of liquid crystalline (LC) compounds with asymmetrical five-membered heterocycle as a central unit. They have a bent shape and are very convenient model-compounds for studying the dependence of the LC properties on the molecular design.
S. I. TORGOVA   +3 more
openaire   +2 more sources

3,5‐Disubstituted‐1,2,4‐oxadiazoles and 4,5‐dihydro‐3,5‐disubstituted‐1,2,4‐oxadiazoles

Journal of Heterocyclic Chemistry, 1978
AbstractA series of 3,5‐disubstituted‐1,2,4‐oxadiazoles (2) were prepared from a mono‐ or dichlorophenyl‐substituted amidoxime and (i) an acid chloride, (ii) an isatoic anhydride, or (iii) a β‐keto ester. Although cyclizations of the same amidoximes with acetaldehyde gave 4,5‐dihydro‐5‐methyl‐substituted derivatives (5), that annulation procedure ...
Harry L. Yale, E. R. Spitzmiller
openaire   +1 more source

Synthesis of 1,2,4‐Oxadiazoles

ChemInform, 2006
AbstractFor Abstract see ChemInform Abstract in Full Text.
L. A. Kayukova, G. I. Gapparova
openaire   +1 more source

1,2,4‐Oxadiazoles

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
openaire   +1 more source

3,3‐Dinitrobutyl‐1,2,4‐oxadiazoles

Journal of Heterocyclic Chemistry, 1980
AbstractThe syntheses of 3,5‐bis(3,3‐dinitrobutyl)‐1,2,4‐oxadiazole and a series of 3‐aryl‐5‐(3,3‐dinitrobutyl)‐1,2,4‐oxadiazoles were accomplished by treating 4,4‐dinitropentanoyl chloride with the appropriate amidoximes to yield the intermediate O‐(4,4‐dinitropentanoyl)amidoximes, which were dehydrated to the 1,2,4‐oxadiazoles.
Mark D. Bjorklund, Michael D. Coburn
openaire   +1 more source

Mass spectrometric analysis of 1,2,4‐Oxadiazoles and 4,5‐Dihydro‐1,2,4‐Oxadiazoles

Mass Spectrometry Reviews, 2004
Abstract1,2,4‐Oxadiazoles and 4,5‐dihydro‐1,2,4‐oxadiazoles are an interesting class of compounds because of their pharmacological and other properties. Although short descriptions of these compounds under mass spectrometric conditions exist, we thought it worthwhile to write a comprehensive review of this class of compounds.
openaire   +2 more sources

A Preferred Synthesis of 1,2,4‐Oxadiazoles

Synthetic Communications, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
Brenda Pipik   +3 more
openaire   +1 more source

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