Dual-Bioorthogonal Molecular Tool: “Click-to-Release” and “Double-Click” Reactivity on Small Molecules and Material Surfaces-Reference-Cited by-同舟云学术

Dual-Bioorthogonal Molecular Tool: “Click-to-Release” and “Double-Click” Reactivity on Small Molecules and Material Surfaces

Published:2019-02-26 Issue:4 Volume:30 Page:1140-1149
ISSN:1043-1802
Container-title:Bioconjugate Chemistry
language:en
Short-container-title:Bioconjugate Chem.

Author:

Luo Wilson¹,Luo Johnny²³,Popik Vladimir V.⁴^ORCID,Workentin Mark S.¹^ORCID

Affiliation:

1. Department of Chemistry and the Centre for Materials and Biomaterials Research, Western University, 1151 Richmond Street, London, Ontario N6A 5B7, Canada

2. Department of Biochemistry, Western University, London, Ontario N6A 5C1, Canada

3. Lawson Health Research Institute, London, Ontario N6C 2R5, Canada

4. Department of Chemistry, University of Georgia, Athens, Georgia 30602, United States

Funder

Natural Sciences and Engineering Research Council of Canada

Division of Chemistry

Western University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.bioconjchem.9b00078

Reference38 articles.

1. Bioorthogonal chemistry: recent progress and future directions

2. Click Chemistry in Complex Mixtures: Bioorthogonal Bioconjugation

3. Cell Surface Engineering by a Modified Staudinger Reaction

4. A Strain-Promoted [3 + 2] Azide−Alkyne Cycloaddition for Covalent Modification of Biomolecules in Living Systems

5. Nitrones as dipoles for rapid strain-promoted 1,3-dipolar cycloadditions with cyclooctynes

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