An entry to 4-aryl-azetidinones via alkylation of nucleophilic arenes using four-membered acyliminium cations
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference39 articles.
1. Discovery of 1-(4-Fluorophenyl)-(3R)-[3-(4-fluorophenyl)-(3S)- hydroxypropyl]-(4S)-(4-hydroxyphenyl)-2-azetidinone (SCH 58235): A Designed, Potent, Orally Active Inhibitor of Cholesterol Absorption
2. Trans diastereoselective synthesis of 3-alkyl substituted β-lactams via the acid chloride-imine reaction of nonactivated acid chlorides
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4. A Novel One-Step Diastereo- and Enantioselective Formation of trans-Azetidinones and Its Application to the Total Synthesis of Cholesterol Absorption Inhibitors
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2. 4-Vinyloxyazetidin-2-one, a Novel Substrate for β-Lactam Synthesis;Beta-Lactams;2017
3. Electrophilic Acylation of Arenes;Side Reactions in Organic Synthesis II;2014-05-30
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5. A Formal Synthesis of Ezetimibe via Cycloaddition/Rearrangement Cascade Reaction;The Journal of Organic Chemistry;2011-07-26
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