A new 31P NMR method for the enantiomeric excess determination of diols and secondary diamines with C2 symmetry
- 1 September 1995
- journal article
- Published by Elsevier in Tetrahedron: Asymmetry
- Vol. 6 (9) , 2353-2356
- https://doi.org/10.1016/0957-4166(95)00311-c
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- A new and efficient method for the resolution of 1,1'-binaphthalene-2,2'-diolThe Journal of Organic Chemistry, 1993
- The use of (4r,5r)-dicarboalkoxy 2-chloro 1,3,2-dioxaphospholanes as new chiral derivatizing agents for the determination of enantiomeric purity of alcohols by 31P NMR.Tetrahedron: Asymmetry, 1992
- NMR determination of enantiomeric purityChemical Reviews, 1991
- Gas Chromatographic Separation of Enantiomers on Cyclodextrin DerivativesAngewandte Chemie International Edition in English, 1990
- A new reagent for a very simple and efficient determination of enantiomeric purity of alcohols by 31P NMRTetrahedron: Asymmetry, 1990
- Direct chirality determination of secondary carbinol by chirality recognition ability of C2 symmetry 1,1'-binaphthyl-2,2'-diyl phosphoryl chlorideJournal of the American Chemical Society, 1990
- Determination of enantiomeric purity of polar substrates with chiral lanthanide NMR shift reagents in polar solventsThe Journal of Organic Chemistry, 1987
- Determination of enantiomeric purities of alcohols and amines by a phosphorus-31 NMR techniqueJournal of the American Chemical Society, 1984
- 2-Chloro-4(R),5(R)-dimethyl-2-oxo-1,3,2-dioxaphospholane, a new chiral derivatizing agentThe Journal of Organic Chemistry, 1984
- Asymmetric Synthesis of Axially Dissymmetric 1,1′-Binaphthyls via an Intramolecular Ullmann Coupling Reaction of (R)- and (S)-2,2′-Bis(1-bromo-2-naphthylcarbonyloxy)-1,1′-binaphthylBulletin of the Chemical Society of Japan, 1981