Enantioselective Construction of 5‐6‐5 Tricyclic Lactone Framework Bearing a Quaternary Bridgehead Carbon via Rh‐Catalyzed Asymmetric [2+2+2] Cycloaddition of Enediynes
Author:
Affiliation:
1. Department of Basic Medicinal Sciences, Graduate School of Pharmaceutical Sciences Nagoya University Furo-cho Chikusa Nagoya 464-8603 Japan
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202100513
Reference92 articles.
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1. Rh‐Catalyzed Cycloaddition of C60 with Enynes: Unveiling the Mechanistic Pathway;Advanced Synthesis & Catalysis;2024-01-04
2. 生物活性分子にみられる多環式骨格の一挙構築を可能にする触媒的環化異性化反応の開発;YAKUGAKU ZASSHI;2023-11-01
3. Construction of Diverse Polycyclic Structures via Group 9 Metal-Catalyzed Cycloisomerization of 1,6-Diyne Derivatives;Journal of Synthetic Organic Chemistry, Japan;2023-02-01
4. Catalytic Enantioselective Construction of 6‐4 Ring‐Junction All‐Carbon Stereocenters and Mechanistic Insights;Chinese Journal of Chemistry;2022-05-31
5. Computational Study of the Rh/phanephos-Catalyzed Enantioselective [2+2+2] Cyclization of Enediyne, Affording Lactone-Fused Cyclohexadiene Bearing a Quaternary Bridgehead Carbon;Bulletin of the Chemical Society of Japan;2022-02-15
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