Synthesis of a designed transmembrane protein by thioether ligation of solubilised segments: Nα-haloacetylated peptides survived resin cleavage using TFA with EDT as scavenger-Reference-Cited by-同舟云学术

Synthesis of a designed transmembrane protein by thioether ligation of solubilised segments: Nα-haloacetylated peptides survived resin cleavage using TFA with EDT as scavenger

Published:1998-07 Issue:27 Volume:39 Page:4929-4932
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Englebretsen Darren R.,Choma Christin T.,Robillard George T.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

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

3. Design and Chemical Synthesis of a Neoprotein Structural Model for the Cytoplasmic Domain of a Multisubunit Cell-Surface Receptor: Integrin .alpha.IIb.beta.3 (Platelet GPIIb-IIIa)

4. A novel thioether linker: Chemical synthesis of a HIV-1 protease analogue by thioether ligation

5. Methodology for chemical synthesis of proteins;Ramage,1996

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