Peptide synthesis. Part 6. Protection of the sulphydryl group of cysteine in solid-phase synthesis using Nα-fluorenylmethoxycarbonylamino acids. Linear oxytocin derivatives-Reference-Cited by-同舟云学术

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Peptide synthesis. Part 6. Protection of the sulphydryl group of cysteine in solid-phase synthesis using Nα-fluorenylmethoxycarbonylamino acids. Linear oxytocin derivatives

Published:1985 Issue:0 Volume: Page:2057-2064
ISSN:0300-922X
Container-title:J. Chem. Soc., Perkin Trans. 1
language:en
Short-container-title:J. Chem. Soc., Perkin Trans. 1

Author:

Atherton Eric,Pinori Masimo,Sheppard Robert C.

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/1985/P1/P19850002057

Cited by 27 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The life and work of Robert (Bob) C. Sheppard;Journal of Peptide Science;2021-10-05

2. Peptide Global Deprotection/Scavenger-Induced Side Reactions;Side Reactions in Peptide Synthesis;2016

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

4. Analysis of functionalized polyethylene terephthalate with immobilized NTPDase and cysteine;Acta Biomaterialia;2009-11

5. Solid phase peptide synthesis utilizing 9-fluorenylmethoxycarbonyl amino acids;International Journal of Peptide and Protein Research;2009-01-12

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