Exploiting Coupling of Boronic Acids with Triols for a pH-Dependent “Click-Declick” Chemistry-Reference-Cited by-同舟云学术

Exploiting Coupling of Boronic Acids with Triols for a pH-Dependent “Click-Declick” Chemistry

Published:2018-07-31 Issue:17 Volume:83 Page:9756-9773
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Golovanov Ivan S.¹,Mazeina Galina S.¹²,Nelyubina Yulia V.³^ORCID,Novikov Roman A.¹^ORCID,Mazur Anton S.⁴,Britvin Sergey N.⁵^ORCID,Tartakovsky Vladimir A.¹,Ioffe Sema L.¹,Sukhorukov Alexey Yu.¹^ORCID

Affiliation:

1. N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Leninsky Prospect, 47, Moscow 119991, Russia

2. Dmitry Mendeleev University of Chemical Technology of Russia, Miusskaya Sq. 9, Moscow 125047, Russia

3. A. N. Nesmeyanov Institute of Organoelement Compounds, Vavilov Str. 28, Moscow 119991, Russia

4. Center for Magnetic Resonance, St. Petersburg State University, University Av. 26, St. Petersburg 198504, Russia

5. Department of Crystallography, St. Petersburg State University, Universitetskaya Nab. 7/9, St. Petersburg 199034, Russia

Funder

Russian Science Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b01296

Reference55 articles.

1. Click Chemistry: Diverse Chemical Function from a Few Good Reactions

2. Click Chemistry, A Powerful Tool for Pharmaceutical Sciences

3. Cu-Catalyzed Azide−Alkyne Cycloaddition

4. Copper-catalyzed azide–alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper(i) acetylides

5. Click Chemistry in Complex Mixtures: Bioorthogonal Bioconjugation

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