Asymmetric total synthesis and antidepressant activity of (−)-sila-mesembranol bearing a silicon stereocenter
Literature Information
Gan Luo, Lingmin Chen, Yi Li, Yu Fan, Duyang Wang, Yufan Yang, Lu Gao, Ruotian Jiang, Zhenlei Song
Asymmetric total synthesis of (−)-sila-mesembranol, the silicon analog of the natural alkaloid (−)-mesembranol has been achieved in 3.3% yield over 11 steps. The chiral silicon center was enantioselectively constructed via the asymmetric expansion of a silacyclobutane ring. The synthetic (−)-sila-mesembranol in mice exhibits better antidepressant effects than its carbon counterpart.
Related Literature
Patiala (Punjab) India. Report of the Chief Chemist for the year ended April 12th, 1940
DOI: 10.1039/AN940650652A
Government of Madras. Annual Report of the Government Analyst to September 30th, 1939
DOI: 10.1039/AN940650601B
International Union of Chemistry. Tenth Report of the Committee on Atomic Weights
DOI: 10.1039/AN940650415A
Proceedings of the Society of Public Analysts and other Analytical Chemists
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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry










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