The First Synthesis of the ABC-Ring System of ‘Upenamide
Author:
Affiliation:
1. Department of Chemistry, University of York, York, YO10 5DD, U.K., and AstraZeneca R&D Charnwood, Medicinal Chemistry, Bakewell Road, Loughborough, Leics LE11 5RH, U.K.
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol701772d
Reference24 articles.
1. ‘Upenamide: An Unprecedented Macrocyclic Alkaloid from the Indonesian Sponge Echinochalina sp.
2. A stannous chloride-induced deacetalisation–cyclisation process to prepare the ABC ring system of 'upenamide
3. Construction of spiro-oxaquinolizidinone framework of Upenamide via organoiron complexes
4. Deacetalisation–bicyclisation routes to novel polycyclic heterocycles using stannous chloride dihydrate
5. Stereoselective Syntheses of the Octahydropyrano[2,3-b]pyridine DE Core of 'Upenamide via a Stannous Chloride-Induced Deacetalisation–Cyclisation Procedure
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