4.8 Article

Synthetic studies on cyathins:: Enantioselective total synthesis of (+)-allocyathin B2

Journal

ORGANIC LETTERS
Volume 6, Issue 26, Pages 4897-4900

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol048010i

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[Graphics] The enantioselective total synthesis of (+)-allocyathin B-2 has been achieved. Our approach features a convergent enantioselective construction of the 5-6-7 tricyclic core system using the originally developed chiral building blocks via asymmetric catalysis, the intramolecular aldol reaction in high yield, successful samarium diiodide-mediated ring expansion, and a newly developed double-bond installation method.

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