De novo synthesis of teleocidin B analogs

Tetrahedron(2010)

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摘要
Teleocidin B analogs have been synthesized in 24 steps and 1.9% overall yield. The key steps include aromatic Claisen rearrangement, intramolecular Heck reaction of a tetra-substituted alkene, and ruthenium (II) catalyzed indole cyclization. Teleocidin and the new analogs promote cell spreading on fibroblast cells that were treated with amino-Nogo, an inhibitor of cell spreading.
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关键词
Teleocidin B,Intramolecular Heck reaction,Claisen rearrangement,Ruthenium catalyzed indole cyclization
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