Studies toward the Total Synthesis of the Cytotoxic Sponge Alkaloid Pyrinodemin A
Organic Letters2001Vol. 3(8), pp. 1145–1148
Citations Over TimeTop 10% of 2001 papers
Abstract
[structure: see text]. The syntheses of the proposed structure of pyrinodemin A (1) and its cis double bond positional isomer (C15'-C16') in racemic form are described. The key reaction involved an intramolecular nitrone/double bond cycloaddition. Our results suggest that neither 1 nor its double positional isomer is the correct structure of pyrinodemin A
Related Papers
- → Prianosin A, a novel antileukemic alkaloid from the okinawan marine sponge Prianos melanos(1987)89 cited
- → Monanchomycalin C, a New Pentacyclic Guanidine Alkaloid from the Far-Eastern Marine Sponge Monanchora Pulchra(2013)28 cited
- → A C-Ring Regioisomer of the Marine Alkaloid Meridine Exhibits Selective In Vitro Cytotoxicity for Solid Tumours(2001)22 cited
- → Sponge (2′,5′)oligoadenylate synthetase activity in the whole sponge organism and in a primary cell culture(2002)9 cited
- → Sponge Cell Adhesions(1978)7 cited