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Noscapine Derivatives as New Chiral Catalysts in Asymmetric Synthesis: Highly Enantioselective Addition of Diethylzinc to Aldehydes

Mohebbi, Maryam and Bararjanian, Morteza and Ebrahimi, Samad N. and Smiesko, Martin and Salehi, Peyman. (2018) Noscapine Derivatives as New Chiral Catalysts in Asymmetric Synthesis: Highly Enantioselective Addition of Diethylzinc to Aldehydes. SYNTHESIS-STUTTGART, 50 (9). pp. 1841-1848.

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Official URL: https://edoc.unibas.ch/64106/

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Abstract

Noscapine, a natural alkaloid, has never been used as a parent scaffold in chiral induction. The first examples of noscapinoid compounds as efficient catalysts in asymmetric synthesis are now reported. Three derivatives of noscapine were synthesized from its reaction with different Grignard reagents. Asymmetric addition of diethylzinc to aldehydes was performed in the presence of these catalysts in high yields and good to excellent ees.
Faculties and Departments:05 Faculty of Science
05 Faculty of Science > Departement Pharmazeutische Wissenschaften
05 Faculty of Science > Departement Pharmazeutische Wissenschaften > Ehemalige Einheiten Pharmazie > Molecular Modeling (Vedani)
05 Faculty of Science > Departement Pharmazeutische Wissenschaften > Pharmazie
UniBasel Contributors:Smiesko, Martin
Item Type:Article, refereed
Article Subtype:Research Article
Publisher:GEORG THIEME VERLAG KG
ISSN:0039-7881
Note:Publication type according to Uni Basel Research Database: Journal article
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Last Modified:28 Apr 2020 09:18
Deposited On:28 Apr 2020 09:18

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