Korbel, Gregory A. et al. published their research in Journal of the American Chemical Society in 2001 | CAS: 156311-83-0

((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0) belongs to triazole derivatives. Triazoles exhibit substantial isomerism, depending on the positioning of the nitrogen atoms within the ring.Triazole heterocyclic structures are found to form many weak nonbond interactions with the receptors and enzymes in biological systems.Application In Synthesis of ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V)

Reaction microarrays: a method for rapidly determining the enantiomeric excess of thousands of samples was written by Korbel, Gregory A.;Lalic, Gojko;Shair, Matthew D.. And the article was included in Journal of the American Chemical Society in 2001.Application In Synthesis of ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) The following contents are mentioned in the article:

This contribution describes a new method that the authors have named reaction microarrays, in which DNA microarray technol. has been adapted to measure the ee of tens of thousands of samples rapidly and en masse. To evaluate the reaction microarray method, α-amino acids were used because of their fundamental chem. and biol. importance, the availability of structural diversity, and their bifunctional structure. Samples of N-Boc-protected α-amino acids were arrayed and covalently attached to amine-functionalized glass slides. Automated contact printing of nanoliter volumes from 2 mM solutions chemoselectively attached <10-11 moles of amino acid to each spot on a glass slide in a spatially arrayed manner. Uncoupled surface amines were acetylated and en masse Boc-deprotection yielded the free amine. In analogy to DNA microarrays, where relative gene expression levels are measured by a ratio of fluorescent reporters, reaction microarrays utilize two fluorescent probes to measure a ratio of enantiomers. This study involved multiple reactions and reactants, such as ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0Application In Synthesis of ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V)).

((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) (cas: 156311-83-0) belongs to triazole derivatives. Triazoles exhibit substantial isomerism, depending on the positioning of the nitrogen atoms within the ring.Triazole heterocyclic structures are found to form many weak nonbond interactions with the receptors and enzymes in biological systems.Application In Synthesis of ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V)

Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics