A highly stereoselective synthesis of s(-)-[1,1′-binaphthalene]-2,2′-diol
- 1 January 1983
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 24 (31) , 3261-3262
- https://doi.org/10.1016/s0040-4039(00)88151-4
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Highly enantioselective reduction of alkynyl ketones by a binaphthol-modified aluminum hydride reagent. Asymmetric synthesis of some insect pheromonesTetrahedron Letters, 1981
- Induction of axial dissymmetry into the 1,1′-binaphthyl bond via an intramolecular ullmann coupling reactionJournal of the Chemical Society, Chemical Communications, 1980
- Asymmetric synthesis via axially dissymetric molecules. 2. A highly efficient synthesis of prostaglandin intermediates possessing the 15S configurationJournal of the American Chemical Society, 1979
- Biomimetic asymmetric oxidative coupling of phenolsBioorganic Chemistry, 1978
- Synthesis and properties of chiral macrotricyclic ligands. Complexation and transport of chiral molecular cations and anionsHelvetica Chimica Acta, 1978
- Host-guest complexation. 7. The binaphthyl structural unit in host compoundsThe Journal of Organic Chemistry, 1977
- Chiral recognition in molecular complexingJournal of the American Chemical Society, 1973
- Enantiomeric cyclic binaphthyl phosphoric acids as resolving agents.Tetrahedron Letters, 1971
- The oxidation of phenols with copper‐amine catalysts and its relation to the mode of action of tyrosinase: I. The catalytic oxidation of monohydric phenols to orthoquinone derivativesRecueil des Travaux Chimiques des Pays-Bas, 1955
- Darstellung von BinaphthylendioxydBerichte der deutschen chemischen Gesellschaft (A and B Series), 1926