Iridium-Catalysed C–H Borylation Facilitates a Total Synthesis of the HRV 3C Protease Inhibitor (±)-Thysanone
Author:
Affiliation:
1. School of Chemical Sciences, The University of Auckland
2. Department of Molecular Biology, The Scripps Research Institute
3. Department of Molecular Medicine and Pathology, The University of Auckland
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0033-1340495.pdf
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1. Metal-catalysed C–H bond activation and borylation;Chemical Society Reviews;2022
2. Understanding the Activation of Air-Stable Ir(COD)(Phen)Cl Precatalyst for C–H Borylation of Aromatics and Heteroaromatics;Organic Letters;2021-02-05
3. The Dötz Benzannulation Reaction: A Booming Methodology for Natural Product Synthesis;ChemistrySelect;2020-05-07
4. Stereoselective Total Synthesis of the Dimeric Naphthoquinonopyrano-γ-lactone (−)-Crisamicin A: Introducing the Dimerization Site by a Late-Stage Hartwig Borylation;Organic Letters;2020-04-16
5. The Pictet–Spengler Reaction: A Powerful Strategy for the Synthesis of Heterocycles;Advances in Heterocyclic Chemistry;2019
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