The effect of the change of synthetic route on the product 7524-52-9

I hope my short article helps more people learn about this compound(H-Trp-OMe.HCl)Category: dioxole. Apart from the compound(7524-52-9), you can read my other articles to know other related compounds.

The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: H-Trp-OMe.HCl(SMILESS: N[C@@H](CC1=CNC2=CC=CC=C12)C(OC)=O.[H]Cl,cas:7524-52-9) is researched.HPLC of Formula: 455-70-9. The article 《Cu(II)-Catalysed Azide-Alkyne Cycloaddition Reaction towards Synthesis of β-Carboline C1-Tethered 1,2,3-Triazole Derivatives》 in relation to this compound, is published in ChemistrySelect. Let’s take a look at the latest research on this compound (cas:7524-52-9).

The synthesis of hybrid mols. containingβ-carboline C1-linked 1,2,3-triazoles I (R1 = H, COOMe, COOEt; R2 = H, Me, Bn, CH2COOEt, etc.; R3 = Ph, n-Bu, COOEt, n-pentyl, CH2OH; R4 = H, COOEt) in moderate to good yields has been described. The developed transformation was realized by using Cu(II)-catalyzed click-reaction of diverse alkynes R3CC R4 with in-situ derived rarely explored β-carboline tethered aliphatic azides II. These mol. hybrids also exhibited excellent fluorescence properties.

I hope my short article helps more people learn about this compound(H-Trp-OMe.HCl)Category: dioxole. Apart from the compound(7524-52-9), you can read my other articles to know other related compounds.

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