O-alkylation of carboxylic acids and phenols with oxaphospholenes: (Preliminary communication)
Author:
Publisher
Wiley
Subject
General Chemistry
Reference5 articles.
1. H.M. Buck W.G. Voncken
2. Stereochemistry of Phosphorus(V) Fluorides
3. Nuclear magnetic resonance evidence for the pathways of pseudorotation in alkyloxyphosphoranes
4. A Crystalline Tetraalkoxyalkylphosphorane from the Reaction of Trimethyl Phosphite with an α,β-Unsaturated Ketone. 3-Benzylidene-2,4-pentanedione. P31 and H1 Nuclear Magnetic Resonance Spectra1,2
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1. Penta co-ordinated organo-phosphorus compounds as model substances for simulation of biochemical conversions. Part I. A model description for the specific interaction t-RNA synthetase-amino acid; a selection procedure;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02
2. 2,2,2-Trimethoxy-5-methyl-Δ4-oxaphospholene 1;Fieser and Fieser's Reagents for Organic Synthesis;2006-12-15
3. N-alkylation of dimethylaniline using 1,3,2-oxaphosphalenes;Bulletin of the Academy of Sciences of the USSR Division of Chemical Science;1979-07
4. Structure of the reaction products of the 2-p-dimethylaminoanil of 1,3-dimethyl-1,2,3-propanetrione with trimethyl phosphite and Tri(dimethylamino)phosphine;Bulletin of the Academy of Sciences of the USSR Division of Chemical Science;1979-02
5. P-Funktionalisierung von ?-Nitrostyrolen mit Trialkylphosphiten;Journal f�r Praktische Chemie;1977
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