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Total Synthesis of Cyrneine A

Elamparuthi, Elangovan and Fellay, Cindy and Neuburger, Markus and Gademann, Karl. (2012) Total Synthesis of Cyrneine A. Angewandte Chemie International Edition, 51 (17). pp. 4071-4073.

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Abstract

Neuritogenic natural products: The tricyclic diterpene cyrneine A featuring a hexatrienal unit was prepared synthetically for the first time by a Heck reaction, a carbene ring expansion, and a reductive carbonylation. The structure of the natural product was assigned by X-ray crystal analysis of a synthetic sample.
Faculties and Departments:05 Faculty of Science
05 Faculty of Science > Departement Chemie > Former Organization Units Chemistry > Organische Chemie (Gademann)
UniBasel Contributors:Gademann, Karl and Neuburger, Markus and Elamparuthi, Elangovan and Elangovan, Elamparuthi
Item Type:Article, refereed
Article Subtype:Research Article
Publisher:Wiley
ISSN:1433-7851
e-ISSN:1521-3773
Note:Publication type according to Uni Basel Research Database: Journal article
Language:English
Identification Number:
Last Modified:04 Oct 2017 12:51
Deposited On:14 Sep 2012 07:16

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