Structural analysis of β-turn mimics containing a substituted 6-aminocaproic acid linker

DOI: 10.1021/ja00124a001

Source and publish data:

Journal of the American Chemical Society p. 5169 - 5178 (1995)

Update date:2022-08-06

Topics:

Authors:

Kitagawa

Vander Velde

Dutta Dutta

Morton Morton

Takusagawa

Aube Aube

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Article abstract of DOI:10.1021/ja00124a001

A series of β-turn models have been prepared consisting of the dipeptide Ala-Gly cyclized with all stereoisomers of 6-amino-3,5-dimethylcaproic acid and 6-amino-3-methylcaproic acid, as were related peptides based on Gly-Gly and Ala-Ala. The requisite lin

Full text of DOI:10.1021/ja00124a001

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