A new protecting group for tryptophan in solid-phase peptide synthesis which protects against acid-catalyzed side reactions and facilitates purification by HPLC-Reference-Cited by-同舟云学术

A new protecting group for tryptophan in solid-phase peptide synthesis which protects against acid-catalyzed side reactions and facilitates purification by HPLC

Published:2009-06 Issue:24 Volume:50 Page:2976-2978
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Wahlström Karolina,Undén Anders

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference18 articles.

1. High-Yield Synthesis and Purification of an α-Helical Transmembrane Domain

2. High-performance liquid chromatographic purification of extremely hydrophobic peptides: transmembrane segments

3. Synthesis of hydrophobic peptides: An Fmoc “solubilising tail” method

4. Boc SPPS of two hydrophobic peptides using a “solubilising tail” strategy: dodecaalanine and chemotactic protein 1042–55

5. An N-terminal method for peptide solubilisation

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4. Protection of the indole nucleus of tryptophan in solid-phase peptide synthesis with a dipeptide that can be cleaved rapidly at physiological pH;Tetrahedron Letters;2011-11

5. Orthogonal Protecting Groups and Side-Reactions in Fmoc/tBu Solid-Phase Peptide Synthesis;Amino Acids, Peptides and Proteins in Organic Chemistry;2011-01-31