α-(carbobenzyloxy)nitroarginyl-ε-(carbobenzyloxy)lysylaspartic acid β-benzyl ester

Base Information

Chemical Name:α-(carbobenzyloxy)nitroarginyl-ε-(carbobenzyloxy)lysylaspartic acid β-benzyl ester
CAS No.:72210-37-8
Molecular Formula:C₃₉H₄₈N₈O₁₂
Molecular Weight:820.857
Hs Code.:

Synonyms:α-(carbobenzyloxy)nitroarginyl-ε-(carbobenzyloxy)lysylaspartic acid β-benzyl ester

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Chemical Property of α-(carbobenzyloxy)nitroarginyl-ε-(carbobenzyloxy)lysylaspartic acid β-benzyl ester

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Technology Process of α-(carbobenzyloxy)nitroarginyl-ε-(carbobenzyloxy)lysylaspartic acid β-benzyl ester

There total 12 articles about α-(carbobenzyloxy)nitroarginyl-ε-(carbobenzyloxy)lysylaspartic acid β-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:

Reference yield: 87.0%

: 191930-78-6
C₅₂H₅₈N₈O₁₂

: 72210-37-8
α-(carbobenzyloxy)nitroarginyl-ε-(carbobenzyloxy)lysylaspartic acid β-benzyl ester

Guidance literature:: With methoxybenzene; trifluoroacetic acid; at 0 ℃; for 0.5h;
DOI:10.1021/jm950803a

Reference yield:

: 107304-39-2
α,ε-dicarbobenzoyloxynitroarginyllysine

: 72210-37-8
α-(carbobenzyloxy)nitroarginyl-ε-(carbobenzyloxy)lysylaspartic acid β-benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: DCC / tetrahydrofuran / 18 h / Ambient temperature

2: Et₃N / tetrahydrofuran / 4 h

3: 87 percent / TFA, anisole / 0.5 h / 0 °C

With methoxybenzene; triethylamine; dicyclohexyl-carbodiimide; trifluoroacetic acid; In tetrahydrofuran;
DOI:10.1021/jm950803a

Reference yield:

: C₃₂H₄₀N₈O₁₁

: 72210-37-8
α-(carbobenzyloxy)nitroarginyl-ε-(carbobenzyloxy)lysylaspartic acid β-benzyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / tetrahydrofuran / 4 h

2: 87 percent / TFA, anisole / 0.5 h / 0 °C

With methoxybenzene; triethylamine; trifluoroacetic acid; In tetrahydrofuran;
DOI:10.1021/jm950803a