Palladium(II)-Catalyzed Michael-Type Addition Reactions Using Aryltin Compounds
- 1 September 2000
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 73 (9), 2149-2155
- https://doi.org/10.1246/bcsj.73.2149
Abstract
No abstract availableThis publication has 35 references indexed in Scilit:
- Carbon−Carbon Bond Forming Solid-Phase ReactionsChemical Reviews, 1999
- The palladium–iminophosphine catalyst for the reactions of organostannanesJournal of Organometallic Chemistry, 1999
- Novel and selective α-substitution of ketones and other carbonyl compounds based on Pd-catalyzed cross coupling of α,β-unsaturated carbonyl derivatives containing α-halogen or α-metal groupsJournal of Organometallic Chemistry, 1999
- Catalytic cross-coupling reactions in biaryl synthesisTetrahedron, 1998
- New perspectives in the cross-coupling reactions of organostannanesPure and Applied Chemistry, 1996
- Solvent-controlled addition of alkynyltins or allylic tins to aldehydes catalyzed by indium trichlorideTetrahedron Letters, 1995
- Diastereo- and enantioselective synthesis of allenylcarbinols through SE2' addition of transient nonracemic propargylic stannanes to aldehydes.The Journal of Organic Chemistry, 1995
- Synthesis of anti-Homoallylic Alcohols and Monoprotected 1,2-Diols through InCl3-Promoted Addition of Allylic Stannanes to AldehydesThe Journal of Organic Chemistry, 1995
- The Palladium‐Catalyzed Cross‐Coupling Reactions of Organotin Reagents with Organic Electrophiles [New Synthetic Methods (58)]Angewandte Chemie International Edition in English, 1986
- The cross-coupling reactions of organic halides with organic derivatives of tin, mercury and copper catalyzed by palladiumJournal of Organometallic Chemistry, 1983