A convenient lactonization of diols to γ- and δ-lactones catalysed by transition metal polyhydrides
- 1 May 1992
- journal article
- Published by Elsevier in Journal of Organometallic Chemistry
- Vol. 429 (2), 269-274
- https://doi.org/10.1016/0022-328x(92)83257-i
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- Enantioselective synthesis of 4-substituted γ-lactonesTetrahedron Letters, 1990
- Lipase-catalyzed preparation of optically active .gamma.-butyrolactones in organic solventsThe Journal of Organic Chemistry, 1990
- A New Synthetic Method for β-Substituted γ-Butyrolactones via Palladium-Catalyzed Reaction of 2-Butene-1,4-diol with Aryl and 1-Alkenyl Halides, and Subsequent OxidationSynlett, 1990
- Highly selective γ-lactone syntheses by intramolecular carbenoid carbon-hydrogen insertion in rhodium(II) carboxylate and rhodium(II) carboxamide catalyzed reactions of diazo estersTetrahedron Letters, 1989
- Lactone synthesis of .alpha.,.omega.-diols with hydrogen peroxide catalyzed by heteropoly acids combined with cetylpyridinium chlorideThe Journal of Organic Chemistry, 1988
- Ruthenium-catalyzed oxidative transformation of alcohols and aldehydes to esters and lactonesThe Journal of Organic Chemistry, 1987
- Iridium pentahydride complex catalyzed dehydrogenation of alcohols in the absence of a hydrogen acceptorTetrahedron Letters, 1987
- Ruthenium complex catalyzed regioselective dehydrogenation of unsymmetrical .alpha.,.omega.-diolsThe Journal of Organic Chemistry, 1986
- Oxidation of primary and secondary alcohols by the catalysis of palladiumThe Journal of Organic Chemistry, 1983
- Ruthenium catalyzed transformation of alcohols to esters and lactonesTetrahedron Letters, 1981