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tert-Butyloxycarbonyl-l-aminosuccinyl-glycyl-l-alanine methyl ester (Boc-l-Asu-Gly-l-Ala-OMe)

✍ Scribed by Capasso, S. ;Mazzarella, L. ;Sica, F. ;Zagari, A.

Book ID: 114504653
Publisher: International Union of Crystallography
Year: 1987
Tongue: English
Weight: 462 KB
Volume: 43
Category: Article
ISSN: 0108-2701
DOI: 10.1107/s0108270187090905

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Solid-state conformations of aminosuccin

Solid-state conformations of aminosuccinyl peptides: structure of tert-butyloxycarbonyl-l-prolyl-l-aminosuccinyl-glycyl-l-alanine methyl ester (Boc-l-Pro-l-Asu-Gly-l-Ala-OMe). A case of psuedo-translational symmetry

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Conformationally restrained peptides: cr

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α-N-tert-Butyloxycarbonyl-l-amino-(N-met

α-N-tert-Butyloxycarbonyl-l-amino-(N-methyl)succinimide (Boc-l-Asu-NMe)

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tert-Butoxycarbonyl-l-leucyl-l-alanine

tert-Butoxycarbonyl-l-leucyl-l-alanine trichloroethyl ester (Boc-l-Leu-l-Ala-OTce)

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The title compound, C 16 H 27 Cl 3 N 2 O 5 , which is an enantiopure dipeptide trichloroethyl ester, adopts an extended conformation. The molecules are linked via -NHÁ Á ÁO C hydrogen bonds into a unique -spiral assembly along the c axis.

Preferred conformations of tert.-butylox

Preferred conformations of tert.-butyloxycarbonyl-L-aminosuccinyl-glycyl-glycine methyl ester in the solid and solution state

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cis- and trans-Conformers at the urethan

cis- and trans-Conformers at the urethane linkage: tert-butoxycarbonyl-l-alanyl-l-proline methyl ester (Boc-l-Ala-l-Pro-OMe)

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