(2S,5S,8S,11S)-1-Acetyl-1,4-diaza-3-keto-5-carboxy-10-thia-tricyclo-[2.8.04,8]-tridecane, 1 synthesis of prolyl-proline-derived, peptide-functionalized templates for α-helix formation-Reference-Cited by-同舟云学术

(2S,5S,8S,11S)-1-Acetyl-1,4-diaza-3-keto-5-carboxy-10-thia-tricyclo-[2.8.04,8]-tridecane, 1 synthesis of prolyl-proline-derived, peptide-functionalized templates for α-helix formation

Published:1988-01 Issue:39 Volume:29 Page:4931-4934
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kemp D.S.,Curran Timothy P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

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4. Conformationally restricted cyclic nonapeptides derived from L-cysteine and LL-3-amino-2-piperidone-6-carboxylic acid (LL-Acp), a potent .beta.-turn-inducing dipeptide analog

5. Amino acid derivatives that stabilized secondary structures of polypeptides—III. β-Enaminonitriles as analogs of secondary amides. The MCC group—1-acylamino-2-aminoalkyl-3-cyano-2-cyclopentenes as amino acid analogs.

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