JOURNAL ARTICLE

N-{N-[N-(1,1-Dimethylethoxycarbonyl)-L-leucyl]-N-methyl-L-leucyl}-N-methyl-L-leucine benzyl ester

Wen XuXiao Jian LiaoJian Zhong DiaoLei ZhouShi Hai Xu

Year: 2008 Journal:   Acta Crystallographica Section E Structure Reports Online Vol: 64 (11)Pages: o2178-o2178   Publisher: International Union of Crystallography

Abstract

The tripeptide title compound, C(32)H(53)N(3)O(6), synthesized in 80% yield by coupling of N-methyl-l-leucine benzyl ester with tert-butoxy-carbonyl-l-leucyl-N-methyl-l-leucine at 273 K, conjugates through two amide linkages and includes two protecting groups: a tert-butyl-oxycarbonyl group at the C-tip and a benzyl group at the N-tip. A classical inter-molecular N-H⋯O hydrogen bond and a weak non-conventional inter-molecular C-H⋯O contact connect the mol-ecules, forming layers parallel to (001).

Keywords:
Tripeptide Amide Chemistry Leucine Stereochemistry Yield (engineering) Hydrogen bond Methyl group Peptide Molecule Medicinal chemistry Group (periodic table) Amino acid Biochemistry Organic chemistry Materials science

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Topics

Carbohydrate Chemistry and Synthesis
Physical Sciences →  Chemistry →  Organic Chemistry
Chemical Synthesis and Analysis
Life Sciences →  Biochemistry, Genetics and Molecular Biology →  Molecular Biology
Crystal structures of chemical compounds
Physical Sciences →  Chemistry →  Inorganic Chemistry

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