Regioselective Formation of Optically Active Cycloheptatrienes by Chiral Tethered Büchner Reaction
- 6 March 2004
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 33 (4) , 404-405
- https://doi.org/10.1246/cl.2004.404
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Highly Stereoselective Protonation of the Enolate of a Bicyclic Cycloheptatrienyl Lactone Occurs on the Hindered FaceOrganic Letters, 2002
- Entropy-Controlled Asymmetric Synthesis. How Differential Activation Entropy Is Induced in Chiral Tethered ReactionsOrganic Letters, 2000
- Dirhodium(II) tetra(triphenylacetate): A highly efficient catalyst for the site-selective intramolecular C-H insertion reactions of α-Diazo β-Keto EstersTetrahedron Letters, 1992
- Cycloheptatriene syntheses through rhodium(II) acetate-catalyzed intramolecular addition reactions of -benzyldiazoacetamidesTetrahedron Letters, 1988
- Transition-metal-catalyzed reactions of diazo compounds. 2. Addition to aromatic molecules: catalysis of Buchner's synthesis of cycloheptatrienesThe Journal of Organic Chemistry, 1981