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N-tert.-butyloxycarbonyl tyrosyl, D-methionyl, glycyl, phenylanalyl, 1-2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl> proline

Base Information
  • Chemical Name:N-tert.-butyloxycarbonyl tyrosyl, D-methionyl, glycyl, phenylanalyl, 1-2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl> proline
  • CAS No.:115615-66-2
  • Molecular Formula:C49H66N6O17S
  • Molecular Weight:1043.16
  • Hs Code.:
N-tert.-butyloxycarbonyl tyrosyl, D-methionyl, glycyl, phenylanalyl, <N<sup>1</sup>-2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl> proline

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Chemical Property of N-tert.-butyloxycarbonyl tyrosyl, D-methionyl, glycyl, phenylanalyl, 1-2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl> proline
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Technology Process of N-tert.-butyloxycarbonyl tyrosyl, D-methionyl, glycyl, phenylanalyl, 1-2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl> proline

There total 9 articles about N-tert.-butyloxycarbonyl tyrosyl, D-methionyl, glycyl, phenylanalyl, 1-2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl> proline which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
Multi-step reaction with 3 steps
1: 55 percent / N-methylmorpholine, isobuthylchlorocarbonate / dimethylformamide / -15 deg C, 1 h then R.T., 2 h
2: hydrogen / 10percent palladium on charcoal / methanol
3: 5 percent / 1-hydroxybenzotriazole, N,N -dicyclohexylcarbodiimide / tetrahydrofuran / -15 deg C, 1 h then R.T., overnight
With 4-methyl-morpholine; hydrogen; benzotriazol-1-ol; dicyclohexyl-carbodiimide; isobutyl chloroformate; palladium on activated charcoal; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;
DOI:10.1016/S0040-4020(01)89802-1
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