Synthesis and application ofNα-Fmoc-Nπ-4-methoxybenzyloxymethylhistidine in solid phase peptide synthesis-Reference-Cited by-同舟云学术

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Synthesis and application ofNα-Fmoc-Nπ-4-methoxybenzyloxymethylhistidine in solid phase peptide synthesis

Published:2012-10-30 Issue:12 Volume:18 Page:763-769
ISSN:1075-2617
Container-title:Journal of Peptide Science
language:en
Short-container-title:J. Pept. Sci.

Author:

Hibino Hajime¹,Miki Yasuyoshi²,Nishiuchi Yuji

Affiliation:

1. SAITO Research Center; Peptide Institute, Inc.; Ibaraki; Osaka; 567-0085; Japan

2. School of Pharmaceutical Sciences; Kinki University; Higashi-Osaka; Osaka; 577-8502; Japan

Publisher

Wiley

Subject

Organic Chemistry,Drug Discovery,Pharmacology,Molecular Biology,Molecular Medicine,General Medicine,Biochemistry,Structural Biology

Reference27 articles.

1. Amino acid-protecting groups;Isidro-Llobet;Chem. Rev.,2009

2. The use of the Nπ-phenacyl group for the protection of the histidine side chain in peptide synthesis;Fletcher;J. Chem. Soc., Perkin Trans. 1,1979

3. An approach to the prevention of racemisation in the synthesis of histidine-containing peptides;Jones;J. Chem. Soc., Chem. Commun.,1978

4. Protection of histidine in peptide synthesis. A reassessment of the trityl group;Sieber;Tetrahedron Lett.,1978

5. Limiting racemization and aspartimide formation in microwave-enhanced Fmoc solid phase peptide synthesis;Palasek;J. Pept. Sci.,2007

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4. Suppression of Simultaneous Fmoc-His(Trt)-OH Racemization and N^α-DIC-Endcapping in Solid-Phase Peptide Synthesis through Design of Experiments and Its Implication for an Amino Acid Activation Strategy in Peptide Synthesis;Organic Process Research & Development;2022-06-27

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