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N(α)-benzyloxycarbonyl-N(ε)-9-fluorenylmethyloxycarbonyl-L-lysine benzyl ester

Base Information Edit
  • Chemical Name:N(α)-benzyloxycarbonyl-N(ε)-9-fluorenylmethyloxycarbonyl-L-lysine benzyl ester
  • CAS No.:827021-73-8
  • Molecular Formula:C36H36N2O6
  • Molecular Weight:592.692
  • Hs Code.:
  • Mol file:827021-73-8.mol
N<sup>(α)</sup>-benzyloxycarbonyl-N<sup>(ε)</sup>-9-fluorenylmethyloxycarbonyl-L-lysine benzyl ester

Synonyms:N(α)-benzyloxycarbonyl-N(ε)-9-fluorenylmethyloxycarbonyl-L-lysine benzyl ester

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Chemical Property of N(α)-benzyloxycarbonyl-N(ε)-9-fluorenylmethyloxycarbonyl-L-lysine benzyl ester Edit
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Technology Process of N(α)-benzyloxycarbonyl-N(ε)-9-fluorenylmethyloxycarbonyl-L-lysine benzyl ester

There total 1 articles about N(α)-benzyloxycarbonyl-N(ε)-9-fluorenylmethyloxycarbonyl-L-lysine benzyl ester 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:
Nα-carbobenzyloxy-Nε-9-fluorenylmethoxycarbonyl-L-lysine; With caesium carbonate; In methanol; at 0 - 20 ℃;
benzyl bromide; In N,N-dimethyl-formamide; at 20 ℃; for 48h;
DOI:10.1021/ja046164n
Guidance literature:
With diethylamine; In dichloromethane; at 20 ℃; for 9h;
DOI:10.1021/ja046164n
Guidance literature:
Multi-step reaction with 2 steps
1: 90 percent / diethylamine / CH2Cl2 / 9 h / 20 °C
2: 72 percent / triethylamine / CH2Cl2 / 6.5 h / 0 - 20 °C
With diethylamine; triethylamine; In dichloromethane;
DOI:10.1021/ja046164n
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