Literature DB >> 7174207

Synthetic approaches to peptide analogues containing 4, 4-difluoro-L-proline and 4-keto-L-proline.

J R Sufrin, T M Balasubramanian, C M Vora, G R Marshall.   

Abstract

An improved synthesis of 4, 4-difluoro-L-proline is described. A key step in this synthesis involves the fluorination of Z-4-keto-L-proline benzyl ester, using diethylaminosulfur trifluoride (DAST), to give the corresponding Z-4, 4-difluoro-L-proline benzyl ester. Preparation of dipeptide derivatives containing 4, 4-difluoro-L-proline has been accomplished by initial synthesis of the corresponding 4-keto-L-proline depeptide derivatives, which were then fluorinated with DAST. A one-step synthesis of Boc-4-keto-L-proline from Boc-4-hydroxy-L-proline by chromium trioxide oxidation is reported. These synthetic procedures should facilitate the preparation of a variety of peptide analogues containing 4, 4-difluoro-L-proline and 4-keto-L-proline.

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Year:  1982        PMID: 7174207     DOI: 10.1111/j.1399-3011.1982.tb03065.x

Source DB:  PubMed          Journal:  Int J Pept Protein Res        ISSN: 0367-8377


  1 in total

1.  4-ketoproline: An electrophilic proline analog for bioconjugation.

Authors:  Amit Choudhary; Kimberli J Kamer; Matthew D Shoulders; Ronald T Raines
Journal:  Biopolymers       Date:  2015-03       Impact factor: 2.505

  1 in total

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