Stereospecific Pd(0)-Catalyzed Arylation of an Allylic Hydroxy Phosphonate Derivative: Formal Synthesis of (S)-(+)-ar-Turmerone
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of MissouriSt. Louis, 8001 Natural Bridge Road, St. Louis, Missouri 63121 cspill@umsl.edu
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo0351318
Reference64 articles.
1. Umpolung in allylic phosphonates. Regioselective reaction of acetoxy allylic phosphonates with nucleophiles catalyzed by palladium(0) complex
2. Umpolung in allylic phosphonates. Regio- and stereo-selective synthesis of (E)-γ-amino-α,β-unsaturated phosphonates by palladium-catalysed reaction of allylic acetoxy phosphonates
3. Regioselective Palladium(0) Catalyzed Amination of Carbonates of Allylic α-Hydroxyphosphonates with Hydroxylamine Derivatives: A Convenient Route to Phosphonic Acids Related to the Antibiotic Fosmidomycin
4. SYNTHESIS OF PHOSPHONIC ACIDS RELATED TO THE ANTIBIOTIC FOSMIDOMYCIN FROM ALLYLIC α- AND γ-HYDROXYPHOSPHONATES
5. A Palladium Catalyzed Synthesis of Precursors of 2-Amino-5-Phosphonopentanoic Acid and Related Compounds
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