Now Is The Time For You To Know The Truth About 7524-52-9

This literature about this compound(7524-52-9)Category: dioxolehas given us a lot of inspiration, and I hope that the research on this compound(H-Trp-OMe.HCl) can be further advanced. Maybe we can get more compounds in a similar way.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: H-Trp-OMe.HCl, is researched, Molecular C12H15ClN2O2, CAS is 7524-52-9, about Synthesis of C-mannosylated glycopeptides enabled by Ni-catalyzed photoreductive cross-coupling reactions, the main research direction is mannosylated glycopeptide synthesis solvent effect; nickel catalyzed photoreductive cross coupling reaction mechanism anomerization; insect hormone solid phase peptide syntheses glycopeptide epitope antibody.Category: dioxole.

The biol. functions of tryptophan C-mannosylation are poorly understood, in part, due to a dearth of methods for preparing pure glycopeptides and glycoproteins with this modification. To address this issue, efficient and scalable methods are required for installing this protein modification. Here, we describe unique Ni-catalyzed cross-coupling conditions that utilize photocatalysis or a Hantzsch ester photoreductant to couple glycosyl halides with (hetero)aryl bromides, thereby enabling the α-C-mannosylation of 2-bromo-tryptophan, peptides thereof, and (hetero)aryl bromides more generally. We also report that 2-(α-D-mannopyranosyl)-L-tryptophan undergoes facile anomerization in the presence of acid: something that must be considered when preparing and handling peptides with this modification. These developments enabled the first automated solid-phase peptide syntheses of C-mannosylated glycopeptides, which we used to map the epitope of an antibody, as well as providing the first verified synthesis of Carmo-HrTH-I, a C-mannosylated insect hormone. To complement this approach, we also performed late-stage tryptophan C-mannosylation on a diverse array of peptides, demonstrating the broad scope and utility of this methodol. for preparing glycopeptides.

This literature about this compound(7524-52-9)Category: dioxolehas given us a lot of inspiration, and I hope that the research on this compound(H-Trp-OMe.HCl) can be further advanced. Maybe we can get more compounds in a similar way.

Reference:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem