Facile Allylative Dearomatization Catalyzed by Palladium
- 1 January 2001
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 123 (4), 759-760
- https://doi.org/10.1021/ja003718n
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Transition-Metal-Mediated Dearomatization ReactionsChemical Reviews, 2000
- Dearomatising cyclisations of lithiated N-benzylbenzamidesChemical Communications, 1999
- Stereoselectivity of the Thia-Sommelet [2,3]-DearomatizationJournal of the American Chemical Society, 1998
- Anionic cyclisations of an N-benzyl naphthamide: a route to benzo[e]isoindolonesChemical Communications, 1998
- Rearrangement of 1-methyl-2-(substituted-phenyl)piperidinium 1-methylides in a neutral mediumThe Journal of Organic Chemistry, 1989
- A mild uncatalysed dearomatisation reactionJournal of the Chemical Society, Perkin Transactions 1, 1989
- Asymmetric addition to chiral naphthyloxazolines. A facile route to 1,1,2-trisubstituted 1,2-dihydronaphthalenes in high enantiomeric excessJournal of the American Chemical Society, 1984
- Novel and regioselective aromatic double substitution involving borate anions and a regio- and stereo-selective route to dihydroaromatic derivativesJournal of the Chemical Society, Chemical Communications, 1974
- Sommelet Rearrangement of Sulfonium SaltsTetrahedron Letters, 1968
- Rearrangement of 2,4,6-Trimethylbenzyltrimethylammonium Ion by Sodium Amide to Form an exo-Methylenecyclohexadieneamine and its Reactions1Journal of the American Chemical Society, 1957