Catalytic Asymmetric Synthesis of Benzobicyclo[3.2.1]octanes.
Autor: | Anif Pasha M; Catalysis Laboratory, School of Chemistry, University of Hyderabad, Hyderabad, 500 046, India., Peraka S; Catalysis Laboratory, School of Chemistry, University of Hyderabad, Hyderabad, 500 046, India., Ramachary DB; Catalysis Laboratory, School of Chemistry, University of Hyderabad, Hyderabad, 500 046, India. |
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Jazyk: | angličtina |
Zdroj: | Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2021 Jul 21; Vol. 27 (41), pp. 10563-10568. Date of Electronic Publication: 2021 Jun 17. |
DOI: | 10.1002/chem.202100985 |
Abstrakt: | Lawsone aldehydes were directly transformed into the biologically important, unique carbon skeleton of chiral methanobenzo[f]azulenes/methanodibenzo[a,d][7]annulenes in high dr and ee and in very good yields by using quinine-thiourea-catalyzed tandem Wittig/intramolecular Michael/intramolecular aldol reactions. This asymmetric catalytic tandem protocol will be highly useful because these final molecules are basic skeletons of important antibiotics. (© 2021 Wiley-VCH GmbH.) |
Databáze: | MEDLINE |
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