Rhodium-catalyzed asymmetric 1,4-addition of 2-alkenyl-1,3,2-benzodioxaboroles to α,β-unsaturated ketones
- 1 November 1998
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 39 (46) , 8479-8482
- https://doi.org/10.1016/s0040-4039(98)01866-8
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Rhodium-Catalyzed Asymmetric 1,4-Addition of Aryl- and Alkenylboronic Acids to EnonesJournal of the American Chemical Society, 1998
- Rhodium-Catalyzed Conjugate Addition of Aryl- or 1-Alkenylboronic Acids to EnonesOrganometallics, 1997
- CatecholboraneTetrahedron, 1976
- Hydroboration. XXXIX. 1,3,2-Benzodioxaborole (catecholborane) as a new hydroboration reagent for alkenes and alkynes. General synthesis of alkane- and alkeneboronic acids and esters via hydroboration. Directive effects in the hydroboration of alkenes and alkynes with catecholboraneJournal of the American Chemical Society, 1975
- Synthesis of Pyrolysis Products of Bisdehydrodihydroenmein. II. : Synthesis of (-)-6-Methyl-7-oxobicyclo [3. 2. 1] octaneYAKUGAKU ZASSHI, 1968