This investigation focused on determining if there was a relationship between electron donating group substituent strength and resulting percent yield values of the 1,3,4-oxadiazole product. The data obtained from this investigation aimed to help chemists better understand the reactivity of the 1,3,4-oxadiazole because of its importance in the realm of drug design and development. In order to accomplish this, electron donating groups with varying pKa values were placed on the 1,3,4-oxadiazole and the resulting percent yields were analyzed for possible trends. The substituents used represented both resonance donating and inductively donating groups and were placed in both ortho and para positions to demonstrate possible steric effects. A dir...
International audienceWe report herein the synthesis of 2,5-diaryl-1,3,4-oxadiazoles containing both...
The relationship between the structure and reactivity of compounds is one of the basic problems of o...
1,2,4-Oxadiazoles experienced an almost 80-year long period of scientific lethargy before they tick...
The goal of this project was to determine the effects that electron withdrawing and electron donatin...
2,5-disubstituted 1,3,4-oxadiazoles are a class of organic compound that are widely used and success...
The work described herein investigates the effects of altering structure upon the reactivity of seve...
Two series of amino-substituted 1,2,4- and 1,3,4-oxadiazole matched compounds were evaluated and fou...
Substituent groups are widely used to take advantage of their electronic and steric proper- ties. Fo...
The objective of this project is to develop a general substrate scope by testing various steric and ...
In the world of pharmaceutical synthesis, research to combat foreign pathogens is always necessary. ...
The given research will investigate synthetic strategies and differential functionalization of 1,3,4...
A structure–property study across a series of donor–acceptor–donor structures composed of mono- and ...
Evaluation of the substituent effect in reaction series is an issue of interest, as it is fundamenta...
For the effective analysis of organic and organoelement reactivity and the reaction mechanisms we ha...
Oxadiazoles are five-membered heteroaromatic rings containing two carbons, two nitrogens, and one ox...
International audienceWe report herein the synthesis of 2,5-diaryl-1,3,4-oxadiazoles containing both...
The relationship between the structure and reactivity of compounds is one of the basic problems of o...
1,2,4-Oxadiazoles experienced an almost 80-year long period of scientific lethargy before they tick...
The goal of this project was to determine the effects that electron withdrawing and electron donatin...
2,5-disubstituted 1,3,4-oxadiazoles are a class of organic compound that are widely used and success...
The work described herein investigates the effects of altering structure upon the reactivity of seve...
Two series of amino-substituted 1,2,4- and 1,3,4-oxadiazole matched compounds were evaluated and fou...
Substituent groups are widely used to take advantage of their electronic and steric proper- ties. Fo...
The objective of this project is to develop a general substrate scope by testing various steric and ...
In the world of pharmaceutical synthesis, research to combat foreign pathogens is always necessary. ...
The given research will investigate synthetic strategies and differential functionalization of 1,3,4...
A structure–property study across a series of donor–acceptor–donor structures composed of mono- and ...
Evaluation of the substituent effect in reaction series is an issue of interest, as it is fundamenta...
For the effective analysis of organic and organoelement reactivity and the reaction mechanisms we ha...
Oxadiazoles are five-membered heteroaromatic rings containing two carbons, two nitrogens, and one ox...
International audienceWe report herein the synthesis of 2,5-diaryl-1,3,4-oxadiazoles containing both...
The relationship between the structure and reactivity of compounds is one of the basic problems of o...
1,2,4-Oxadiazoles experienced an almost 80-year long period of scientific lethargy before they tick...