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Solid-phase synthesis of diverse peptide tertiary amides by reductive amination.

ABSTRACT: The synthesis of libraries of conformationally constrained peptide-like oligomers is an important goal in combinatorial chemistry. In this regard an attractive building block is the N-alkylated peptide, also known as a peptide tertiary amide (PTA). PTAs are conformationally constrained because of allylic 1,3 strain interactions. We report here an improved synthesis of these species on solid supports through the use of reductive amination chemistry using amino acid-terminated, bead-displayed oligomers and diverse aldehydes. The utility of this chemistry is demonstrated by the synthesis of a library of 10,000 mixed peptoid-PTA oligomers.

SUBMITTER: Pels K

PROVIDER: S-EPMC4447181 | biostudies-literature | 2015 Mar

REPOSITORIES: biostudies-literature

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Solid-phase synthesis of diverse peptide tertiary amides by reductive amination.

Pels Kevin K Kodadek Thomas T

ACS combinatorial science 20150225 3

The synthesis of libraries of conformationally constrained peptide-like oligomers is an important goal in combinatorial chemistry. In this regard an attractive building block is the N-alkylated peptide, also known as a peptide tertiary amide (PTA). PTAs are conformationally constrained because of allylic 1,3 strain interactions. We report here an improved synthesis of these species on solid supports through the use of reductive amination chemistry using amino acid-terminated, bead-displayed olig ...[more]

PMID: 25695359

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