Uncovering a Latent Ligation Site for Glycopeptide Synthesis
2008; Wiley; Volume: 47; Issue: 29 Linguagem: Inglês
10.1002/anie.200801097
ISSN1521-3773
AutoresRyo Okamoto, Yasuhiro Kajihara,
Tópico(s)Carbohydrate Chemistry and Synthesis
ResumoAngewandte Chemie International EditionVolume 47, Issue 29 p. 5402-5406 Communication Uncovering a Latent Ligation Site for Glycopeptide Synthesis† Ryo Okamoto, Ryo Okamoto International Graduate School of Arts and Sciences, Yokohama City University, 22-2, Seto, Kanazawa-ku, Yokohama, 236-0027 (Japan), Fax: (+81) 45-787-2413Search for more papers by this authorYasuhiro Kajihara Prof. Dr., Yasuhiro Kajihara Prof. Dr. [email protected] International Graduate School of Arts and Sciences, Yokohama City University, 22-2, Seto, Kanazawa-ku, Yokohama, 236-0027 (Japan), Fax: (+81) 45-787-2413Search for more papers by this author Ryo Okamoto, Ryo Okamoto International Graduate School of Arts and Sciences, Yokohama City University, 22-2, Seto, Kanazawa-ku, Yokohama, 236-0027 (Japan), Fax: (+81) 45-787-2413Search for more papers by this authorYasuhiro Kajihara Prof. Dr., Yasuhiro Kajihara Prof. Dr. [email protected] International Graduate School of Arts and Sciences, Yokohama City University, 22-2, Seto, Kanazawa-ku, Yokohama, 236-0027 (Japan), Fax: (+81) 45-787-2413Search for more papers by this author First published: 07 July 2008 https://doi.org/10.1002/anie.200801097Citations: 62 † Financial support from the Japan Society for the Promotion of Science (Grant-in-Aid for Creative Scientific Research no. 17GS0420) is acknowledged. Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat Graphical Abstract Serine in site: A native chemical ligation concept at the serine site is described (see picture). This method was achieved by the CNBr conversion reaction from methylcysteine, which could be obtained by selective S methylation. This new method allowed a consensus sequence that is generally incorporated in N-linked oligosaccharides to be used as a ligation site in the course of glycopeptide synthesis. 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