Results 121 to 130 of about 64,409 (320)

Studies on Pyrazolones. X. Reactions of Pyrazole Blue with Cyanoacetamide and Malononitrile. [PDF]

open access: bronze, 1956
Gunnel Westöö   +4 more
openalex   +1 more source

Combined Inductive and Dispersion Effects Enhance Bioorthogonal Reactivity of Tetrazines Toward Isonitriles

open access: yesAngewandte Chemie International Edition, EarlyView.
Bulky, electron‐withdrawing substituents can significantly enhance the reactivity and stability of tetrazines toward isonitriles, addressing a key challenge in bioorthogonal chemistry. This study explores the role of frontier‐orbital interactions, dispersion forces, and molecular conformation in optimizing tetrazine performance, leading to highly ...
Suprakash Biswas   +5 more
wiley   +1 more source

3,5-Bis(2,4-dinitrophenyl)-4-nitro-1H-pyrazole acetone monosolvate

open access: yesActa Crystallographica Section E, 2012
The title structure, C15H7N7O10·C3H6O, was prepared by pentanitration of 3,5-diphenyl-1H-pyrazole. The proton attached to a pyrazole N atom forms a hydrogen bond with the O atom of the acetone solvent molecule, owing to the NO2 enhanced acidity ...
Logesh Mathivathanan
doaj   +1 more source

Pyrazole Studies. XI. Oxidation by Air of 1:4-Disubstituted Pyrazolidine-3:5-diones. [PDF]

open access: bronze, 1958
Stig Veibel   +5 more
openalex   +1 more source

Kinetics of deuteration of pyrazole [PDF]

open access: yesThe Journal of Organic Chemistry, 1970
Wu, E. C., Vaughan, John D.
openaire   +2 more sources

Expanding the Repertoire of Photoswitchable Unnatural Amino Acids for Enzyme Engineering

open access: yesAngewandte Chemie International Edition, EarlyView.
Enzyme engineering with photoswitchable unnatural amino acids (psUAAs) has a high potential for applications such as biocatalysis. Here, we extend the current repertoire of psUAAs to include more versatile properties paving the way to more advanced photocontrol engineering.
Caroline Hiefinger   +11 more
wiley   +1 more source

1-[1-(3-Methylphenyl)-5-phenyl-4-phenylsulfonyl-1H-pyrazol-3-yl]ethanone

open access: yesActa Crystallographica Section E, 2011
Both the acetyl and phenyl substituents of the central pyrazole ring in the title compound, C24H20N2O3S, are twisted with respect to the pyrazole ring, with the twist involving the phenyl ring being greater [67.4 (1) and 29.6 (2)&#
Mohamed Ghazzali   +3 more
doaj   +1 more source

Pyrazole Studies. XII. Hydrazobenzene-catalysed Oxidation of 1:2-Diphenyl-4-butylpyrazolidine-3,5-dione (Butazolidine). [PDF]

open access: bronze, 1958
Stig Veibel   +5 more
openalex   +1 more source

ALTERATION OF THE RESPONSE OF PLATELETS TO SURFACE STIMULI BY PYRAZOLE COMPOUNDS [PDF]

open access: bronze, 1967
MA Packham   +4 more
openalex   +1 more source

Home - About - Disclaimer - Privacy