An Efficient Preparation of β-Aryl-β-ketophosphonates by the TFAA/H3PO4-Mediated Acylation of Arenes with Phosphonoacetic Acids
Author:
Affiliation:
1. Process Chemistry, Neurogen Corporation, Branford, Connecticut 06405
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo800973e
Reference28 articles.
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2. The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspects
3. Zinc-Mediated Chain Extension of β-Keto Phosphonates
4. Catalytic asymmetric addition of β-keto phosphonates to an activated imine—formation of optically active functionalized phosphonate α-amino acid derivatives
5. A Facile Approach to Alkyl- and Aryl-Substituted 3-Furylphosphonates Based on Ceric Ammonium Nitrate-Promoted Radical Reactions
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