Total synthesis of (+)-desoxoprosopinine via the intramolecular reaction of γ-aminoallylstannane
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference18 articles.
1. Stereocontrolled intramolecular cyclization of ω-tributylstannyl ether aldehydes. synthesis of the 6·7·7·6 ring system of polycyclic ethers
2. Cyclic transition state in the acid catalyzed intramolecular allylstannane-aldehyde condensation
3. Stereocontrolled synthesis of the hemibrevetoxin ring system via an allylic tin method
4. STEREOCONTROLLED SYNTHESIS OF THE 6-7-7-6 RING SYSTEM OF POLYCYCLIC ETHERS VIA THE INTRAMOLECULAR REACTION WITH ω-TRIBUTYLSTANNYL ETHER ALDEHYDES
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1. Hydroformylation in Natural Product Synthesis;Topics in Current Chemistry;2013
2. A Short and Efficient Total Synthesis of (+)-Deoxoprosopinine via Diastereoselective Allylation of the Bicyclic N-Acyl Iminium Ion Formed in situ with a π-Nucleophile;Synlett;2012-11-09
3. ChemInform Abstract: Total Synthesis of (+)-Desoxoprosopinine via the Intramolecular Reaction of γ-Aminoallylstannane.;ChemInform;2010-06-24
4. A Configurational Switch Based on Iridium-Catalyzed Allylic Cyclization: Application in Asymmetric Total Syntheses of Prosopis, Dendrobate, and Spruce Alkaloids;Chemistry - A European Journal;2009-10-12
5. Generation and α-hydroxyalkylation of a novel 3-piperidinol N-α-carbanion intermediate;Science in China Series B: Chemistry;2009-10
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