Immobilized N-chlorosuccinimide as a friendly peptide disulfide-forming reagent.

Abstract:

:A novel immobilized N-chlorosuccinimide resin was developed for peptide disulfide bond formation in combinatorial libraries. The resin is prepared in a simple two-step process from commercial starting materials. Disulfide formation is initiated by adding a peptide solution to the resin, and excess reagent is removed by a convenient filtration upon completion of disulfide formation. Completion of disulfide formation is rapid and clean, as demonstrated by the oxidation of a small nonapeptide library. This immobilized reagent allows a wider scope for the use of N-chlorosuccinimide-based disulfide formation in combinatorial chemistry.

journal_name

ACS Comb Sci

authors

Postma TM,Albericio F

doi

10.1021/co500003p

subject

Has Abstract

pub_date

2014-04-14 00:00:00

pages

160-3

issue

4

eissn

2156-8952

issn

2156-8944

journal_volume

16

pub_type

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