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Updated: Jul 12, 2026

Efficient Construction of Drug-like Bispirocyclic Scaffolds Via Organocatalytic Cycloadditions of α-Imino γ-Lactones and Alkylidene Pyrazolones
10:17

Efficient Construction of Drug-like Bispirocyclic Scaffolds Via Organocatalytic Cycloadditions of α-Imino γ-Lactones and Alkylidene Pyrazolones

Published on: February 7, 2019

(+) -フロンドーシンAの全合成 Ru-触媒化された [5+2] サイクロアディションの適用

Barry M Trost1, Yimin Hu, Daniel B Horne

  • 1Department of Chemistry, Stanford University, Stanford, California 94305-5080, USA. bmtrost@stanford.edu

Journal of the American Chemical Society
|September 1, 2007
PubMed
まとめ

(+) -フロンドーシンAの最初の完全合成は,新しいRu-触媒化された [5+2]サイクル添加を用いて達成されました. この研究は,この天然製品の絶対的な構成を確立します.

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