The β-2,4-dimethyl-3-pentyl ester as a new protecting group for aspartic acid that prevents base-catalyzed aspartimide formation in solid phase peptide synthesis-Reference-Cited by-同舟云学术

The β-2,4-dimethyl-3-pentyl ester as a new protecting group for aspartic acid that prevents base-catalyzed aspartimide formation in solid phase peptide synthesis

Published:1995-05 Issue:22 Volume:36 Page:3909-3912
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Karlström Amelie H.,Undén Anders E.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference7 articles.

1. SIDE REACTIONS IN PEPTIDE SYNTHESIS

2. SOLID PHASE SYNTHESIS OF BOVINE PITUITARY GROWTH HORMONE-(123-131) NONAPEPTIDE

3. Deamidation, isomerization, and racemization at asparaginyl and aspartyl residues in peptides. Succinimide-linked reactions that contribute to protein degradation.

4. Formation of aspartimide peptides in Asp-Gly sequences

5. Succinimide Formation from Aspartyl and Asparaginyl Peptides as a Model for the Spontaneous Degradation of Proteins

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