Highly Efficient and Stereoselective Mukaiyama Aldol Reaction with Chiral Aziridine‐2‐carboxaldehyde and Its Synthetic Applications
Author:
Affiliation:
1. Department of Chemistry Hankuk University of Foreign Studies 17035 Yongin (Republic of Korea
Funder
National Research Foundation of Korea
Publisher
Wiley
Subject
Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajoc.202100567
Reference72 articles.
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2. Recent Advances in Substrate-Controlled Asymmetric Induction Derived from Chiral Pool α-Amino Acids for Natural Product Synthesis
3. Amino acid chirons: a tool for asymmetric synthesis of heterocycles
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1. Comprehensive Insight into Synthetic Strategies of Enigmol and Its Analogs as Therapeutic Agents;Mini-Reviews in Organic Chemistry;2023-11
2. Regioselective ring opening of aziridine for synthesizing azaheterocycle;Frontiers in Chemistry;2023-10-19
3. Mukaiyama aldol reaction: an effective asymmetric approach to access chiral natural products and their derivatives/analogues;RSC Advances;2023
4. Preparation of Enantiopure Non-Activated Aziridines and Synthesis of Biemamide B, D, and <em>epiallo</em>-Isomuscarine;Journal of Visualized Experiments;2022-06-13
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