Cyclohexenone Annelation by Alkylidene C−H Insertion: Synthesis of Oxo-T-cadinol
- 1 January 1996
- journal article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 61 (6) , 2081-2084
- https://doi.org/10.1021/jo951949k
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Intramolecular C-H Insertion by an Alkylidene Carbene: Diastereoselective Synthesis of a Taxol A Ring SynthonThe Journal of Organic Chemistry, 1994
- Quenched molecular dynamics simulations of tuftsin and proposed cyclic analogsJournal of Medicinal Chemistry, 1992
- T-Cadinol: A Pharmacologically Active Constituent of Scented Myrrh: Introductory Pharmacological Characterization and High Field1H- and13C-NMR DataPlanta Medica, 1991
- Intramolecular carbon-hydrogen insertions of alkylidenecarbenes. I. SelectivityThe Journal of Organic Chemistry, 1983
- Molecular sieve-assisted oxidations: new methods for carbohydrate derivative oxidationsJournal of the Chemical Society, Chemical Communications, 1980
- A highly selective method for α-alkylation of ketones potassium enoxytrialkylboratesTetrahedron Letters, 1979
- Oxidative Deoximation with Pyridinium ChlorochromateSynthesis, 1978
- The photochemical total synthesis of(±)-3-OXO-α-cadinol and (±)-α-cadinolTetrahedron Letters, 1977
- Organocuprates. Stereoselective synthesis of axial alcoholsJournal of the American Chemical Society, 1975
- Pyridinium chlorochromate. An efficient reagent for oxidation of primary and secondary alcohols to carbonyl compoundsTetrahedron Letters, 1975