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Journal of Carbohydrate Chemistry Volume 34, 2015 - Issue 1

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Original Articles

Synthesis of Fmoc-Thr Unit Carrying Core 1 O-Linked Sugar With Acid-Sensitive O-Protecting Group and Its Application to the Synthesis of Glycosylated Peptide Thioester

Yuya AsahinaInstitute for Protein Research, Osaka University, Osaka565-0871, Japan

Rina FujimotoDepartment of Applied Biochemistry, Tokai University, Kanagawa259-1292, Japan

Akemi SuzukiInstitute of Glycoscience, Tokai University, Kanagawa259-1292, Japan

Hironobu HojoInstitute for Protein Research, Osaka University, Osaka565-0871, JapanCorrespondence[email protected]

Pages 12-27 | Received 19 Aug 2014, Accepted 14 Oct 2014, Published online: 31 Dec 2014

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https://doi.org/10.1080/07328303.2014.977909
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Bingjia Yan, Wenyi Li & Christian P. R. Hackenberger. (2021) A silyl ether-protected building block for O -GlcNAcylated peptide synthesis to enable one-pot acidic deprotection . Organic & Biomolecular Chemistry 19:37, pages 8014-8017.
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Shun Ito, Yuya Asahina & Hironobu Hojo. (2021) Investigation of protecting group for sialic acid carboxy moiety toward sialylglycopeptide synthesis by the TFA-labile protection strategy. Tetrahedron 97, pages 132423.
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Tomohiro Tanaka, Mika Shiraishi, Akio Matsuda & Mamoru Mizuno. (2019) Efficient synthesis of N- and O-linked glycopeptides using acid-labile Boc groups for the protection of carbohydrate moieties. Tetrahedron Letters 60:40, pages 151106.
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Kazutada Ikeuchi, Kentaro Murasawa, Kenya Ohara & Hidetoshi Yamada. (2019) p -Methylbenzyl Group: Oxidative Removal and Orthogonal Alcohol Deprotection . Organic Letters 21:17, pages 6638-6642.
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Nikesh Narang, Rohit K. Sharma & Hironobu Hojo. 2019. Synthetic Glycomes. Synthetic Glycomes 151 171 .

Yuya Asahina, Toru Kawakami & Hironobu Hojo. (2019) Glycopeptide Synthesis Based on a TFA-Labile Protection Strategy and One-Pot Four-Segment Ligation for the Synthesis of O-Glycosylated Histone H2A. European Journal of Organic Chemistry 2019:9, pages 1915-1920.
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Naoki Takeda, Toshiki Takei, Yuya Asahina & Hironobu Hojo. (2018) Sialyl Tn Unit with TFA‐Labile Protection Realizes Efficient Synthesis of Sialyl Glycoprotein. Chemistry – A European Journal 24:11, pages 2593-2597.
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Patrick K. Chaffey, Xiaoyang Guan, Yaohao Li & Zhongping Tan. (2018) Using Chemical Synthesis To Study and Apply Protein Glycosylation. Biochemistry 57:4, pages 413-428.
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Yusuke Tomabechi, Toshihiko Katoh, Munetaka Kunishima, Toshiyuki Inazu & Kenji Yamamoto. (2017) Chemo-enzymatic synthesis of a glycosylated peptide containing a complex N-glycan based on unprotected oligosaccharides by using DMT-MM and Endo-M. Glycoconjugate Journal 34:4, pages 481-487.
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Hironobu Hojo. (2016) Toward the Understanding of Glycoprotein through Chemical Synthesis. Journal of Synthetic Organic Chemistry, Japan 74:10, pages 984-992.
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Hironobu Hojo. (2016) A strategy for the synthesis of hydrophobic proteins and glycoproteins. Organic & Biomolecular Chemistry 14:27, pages 6368-6374.
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Yuya Asahina, Shinobu Komiya, Ami Ohagi, Rina Fujimoto, Hiroko Tamagaki, Katsuhiro Nakagawa, Takashi Sato, Shizuo Akira, Toshifumi Takao, Akira Ishii, Yoshiaki Nakahara & Hironobu Hojo. (2015) Chemical Synthesis of O‐Glycosylated Human Interleukin‐2 by the Reverse Polarity Protection Strategy. Angewandte Chemie International Edition 54:28, pages 8226-8230.
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N.K. Terrett. (2015) Combinatorial Chemistry Online Volume 17, Issue 4, April 2015. Combinatorial Chemistry - an Online Journal 17:4, pages 13-15.
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Synthesis of Fmoc-Thr Unit Carrying Core 1 O-Linked Sugar With Acid-Sensitive O-Protecting Group and Its Application to the Synthesis of Glycosylated Peptide Thioester

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Synthesis of Fmoc-Thr Unit Carrying Core 1 O-Linked Sugar With Acid-Sensitive O-Protecting Group and Its Application to the Synthesis of Glycosylated Peptide Thioester

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