相关实验视频

Updated: Mar 17, 2026

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

Published on: February 7, 2019

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不高效C1对称二烯的结构调整,以实现高效的恩选择性氧化器官催化

Kondapalli Pavankumar1, Rajendra P Shirke1, Kang Kim1

  • 1Gachon Institute of Pharmaceutical Science & Department of Pharmacy, College of Pharmacy, Gachon University, 191 Hambakmoeiro, Yeonsu-gu, Incheon 21936, Republic of Korea.

ACS omega
|March 16, 2026
PubMed
概括

一种新型的C1-对称二烯催化剂能够实现对抗选择性氧化转化,在子α-托西化中实现高产量和对抗选择性. 这种C1设计的性能优于C2类似物,在性高性催化中取得了显著的进步.

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