Use of Acid-labile Protective Groups for Carbohydrate Moieties in Synthesis of Glycopeptides Related to Type II Collagen-Reference-Cited by-同舟云学术

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Use of Acid-labile Protective Groups for Carbohydrate Moieties in Synthesis of Glycopeptides Related to Type II Collagen

Published:1998-07-30 Issue:31 Volume:54 Page:12047-12070
ISSN:0040-4020
Container-title:Tetrahedron
language:
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Author:

Broddefalk J

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Cited by 24 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. Photo-induced radical thiol–ene chemistry: a versatile toolbox for peptide-based drug design;Chemical Society Reviews;2021

2. Diastereoselective Synthesis of Axially Chiral Xylose-Derived 1,3-Disubstituted Alkoxyallenes: Scope, Structure, and Mechanism;The Journal of Organic Chemistry;2020-07-23

3. Modulation of receptor binding to collagen by glycosylated 5‐hydroxylysine: Chemical biology approaches made feasible by Carpino's Fmoc group;Peptide Science;2020-03-19

4. Conformationally Switchable Glycosyl Donors;The Journal of Organic Chemistry;2019-10-04

5. Efficient synthesis of N- and O-linked glycopeptides using acid-labile Boc groups for the protection of carbohydrate moieties;Tetrahedron Letters;2019-10

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