Etude conformationnelle de β-hydroxyphosphonates par R.M.N. mise en evidence d'un couplage stereospecifique en W 31P-C-C-O-1H
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. Steric requirements of 4JH-C-C-O-H- and 4JH-C-C-S-H-couplings
2. Hydroxyl proton magnetic resonance study of aliphatic alcohols
3. Structures and reactions of condensation products of benzaldehyde and acetoacetic ester
4. Assignment of configurations of some dimethyl bicyclo[2.2.1] phosphonates by NMR. W-type 31C-C-C-1 couplings
5. The mechanism of the Horner–Emmons modification of the Wittig reaction
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1. NEW TRI-COORDINATED AND PENTACOORDINATED PHOSPHORUS COMPOUNDS AND A BORON SPIRANE INVOLVING AN ENOLPYRUVATE MOIETY. SYNTHESIS OF A HYDROXYPHOSPHORANE MODEL OF INTERMEDIATE PHOSPHORANES IN NUCLEOPHILIC SUBSTITUTION REACTIONS ON PHOSPHORIC ESTERS OF ENOLPYRUVIC ACID;Phosphorus and Sulfur and the Related Elements;1988-01-01
2. 1H NMR spectra and stereochemistry of diastereomeric 2-arylamino-1,2-diarylethanephosphonic acid esters;Journal of Molecular Structure;1982-09
3. SPIROPHOSPHORANYLATION D'HYDROXYACIDES NATURELS (ACIDES MALIQUE, CITRIQUE ET TARTRIQUE)—EMETIQUES PHOSPHORES ET OLIGOMERES A PHOSPHORE PENTA ET HEXACOORDINE;Phosphorus and Sulfur and the Related Elements;1981-08
4. Preparation et proprietes de quelques sulfures de phospholes fonctionnels;Tetrahedron;1974-01
5. Effet de structure sur la reversibilite de la condensation aldolique;Tetrahedron;1973-12
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