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Diastereoselective Construction of Quaternary Carbons Directed via Macrocyclic Ring Conformation: Formal Synthesis of (−)-Mesembrine

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NIAID Data Ecosystem2026-03-06 收录
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In this article, we report a highly diastereoselective new method for the generation of quaternary carbon centers through an anionic oxy-Cope/alkylation sequence where the diastereoselectivity is induced by the conformation of a macrocyclic tetrasubstituted enolate. The use of our methodology culminated in the formal total synthesis of (−)-mesembrine (34) in 11 steps from known starting materials.

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2016-06-03
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