Thiolate-mediated reductive cyclization: asymmetric total synthesis of (+)-engelharquinone
Author:
Affiliation:
1. Department of Chemistry, Tokyo Institute of Technology, Tokyo, Japan
Publisher
Informa UK Limited
Subject
Inorganic Chemistry,Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/10426507.2019.1603718
Reference6 articles.
1. Secondary metabolites from the roots of Engelhardia roxburghiana and their antitubercular activities
2. Toward Naphthocyclinones: Doubly Connected Octaketide Dimers with a Bicyclo[3.2.1]octadienone Core by Thiolate-Mediated Cyclization
3. Enantioselective Access to Bicyclo[3.2.1]octadienone Skeleton: Total Syntheses of (+)-Engelharquinone and Its Epoxide
4. Asymmetric 1,4-Addition of Organoboron Reagents to Quinone Monoketals Catalyzed by a Chiral Diene/Rhodium Complex: A New Synthetic Route to Enantioenriched 2-Aryltetralones
5. A Diels-Alder Reaction for the Total Synthesis of the Novel Antibiotic Antitumor Agent Mensacarcin
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