Solid phase peptide synthesis
Author:
Publisher
Elsevier
Reference76 articles.
1. Therapeutic peptides;Albericio;Future Medicinal Chemistry,2012
2. Orthogonal protecting groups for Nα-amino and C-terminal carboxyl functions in solid-phase peptide synthesis;Albericio;Biopolymers Peptide Science,2000
3. Preparation of the very acid-sensitive Fmoc-Lys(Mtt) –OH application in the synthesis of side-chain to side-chain cyclic peptides and oligolysine cores suitable for the solid-phase assembly of MAPs and TASPs;Aletras;International Journal of Peptide and Protein Research,1995
4. A mild procedure for solid phase peptide synthesis: use of fluorenylmethoxycarbonylamino-acids;Atherton;Journal of the Chemical Society. Chemical Communications,1978
5. Side chain protected Nα-fluorenylmethoxycarbonylamino-acids for solid phase peptide synthesis. Nα-fluorenylmethoxycarbonyl-NG-4-methoxy-2,3,6-trimethylbenzenesulphonyl-L-arginine;Atherton;Journal of the Chemical Society, Chemical Communications,1983
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