Efficient Organocatalytic Michael Addition Reaction of β−Ketoesters under High Pressure
Author:
Publisher
The Japan Institute of Heterocyclic Chemistry
Subject
Organic Chemistry,Pharmacology,Analytical Chemistry
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Steglich’s Base Catalyzed Three-Component Synthesis of Isoxazol-5-Ones;Polycyclic Aromatic Compounds;2022-04-07
2. High‐Pressure‐Mediated Thiourea‐Organocatalyzed Asymmetric Michael Addition to (Hetero)aromatic Nitroolefins: Prediction of Reaction Parameters by PCP‐SAFT Modelling;ChemPlusChem;2020-06
3. Enantioselective Synthesis of Quaternary Carbon Stereogenic Centers through the Primary Amine-Catalyzed Michael Addition Reaction of α-Substituted Cyclic Ketones at High Pressure;European Journal of Organic Chemistry;2015-06-05
4. ChemInform Abstract: High-Pressure Organic Chemistry. Part 38. Efficient Organocatalytic Michael Addition Reaction of β-Ketoesters under High Pressure.;ChemInform;2014-02-27
5. Asymmetric organocatalytic desymmetrization of 4,4-disubstituted cyclohexadienones at high pressure: a new powerful strategy for the synthesis of highly congested chiral cyclohexenones;Org. Biomol. Chem.;2014
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