Category: triazolesIn 2020 ,《Synthetic hyperacetylation of nucleosomal histones》 was published in RSC Chemical Biology. The article was written by Kajino, Hidetoshi; Nagatani, Tomomi; Oi, Miku; Kujirai, Tomoya; Kurumizaka, Hitoshi; Nishiyama, Atsuya; Nakanishi, Makoto; Yamatsugu, Kenzo; Kawashima, Shigehiro A.; Kanai, Motomu. The article contains the following contents:
We report combinations of a DMAP-based catalyst and Ph acetate with optimal electron d. as a new chem. system for high-yield, selective synthetic acetylation of histone lysine residues. The utility of this chem. system as a unique biol. tool is demonstrated by applying it to Xenopus laevis sperm chromatin. After reading the article, we found that the author used Tris((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)amine(cas: 510758-28-8Category: triazoles)
Tris((1-benzyl-1H-1,2,3-triazol-4-yl)methyl)amine(cas: 510758-28-8) is a polytriazolylamine ligand which stabilizes Cu(I) towards disproportionation and oxidation thus enhancing its catalytic effect in the azide-acetylene cycloaddition.Category: triazoles
Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics