Metallo-Aldehyde Enolates via Enal Hydrogenation: Catalytic Cross Aldolization with Glyoxal Partners As Applied to the Synthesis of 3,5-Disubstituted Pyridazines
- 22 January 2004
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 69 (4) , 1380-1382
- https://doi.org/10.1021/jo030310a
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- A New Catalytic C-C Bond‐Forming Hydrogenation: Reductive Coupling of Dienes and Glyoxals under Catalytic Hydrogenation ConditionsAngewandte Chemie International Edition in English, 2003
- First Catalytic Reductive Coupling of 1,3-Diynes to Carbonyl Partners: A New Regio- and Enantioselective C−C Bond Forming HydrogenationJournal of the American Chemical Society, 2003
- The Direct Catalytic Asymmetric Cross‐Aldol Reaction of AldehydesAngewandte Chemie International Edition in English, 2003
- Reductive Generation of Enolates from Enones Using Elemental Hydrogen: Catalytic C−C Bond Formation under Hydrogenative ConditionsJournal of the American Chemical Society, 2002
- The First Catalytic, Diastereoselective, and Enantioselective Crossed-Aldol Reactions of AldehydesAngewandte Chemie International Edition in English, 2001
- Synthesis and Reactions of Haloazodienes. A New and General Synthesis of Substituted PyridazinesThe Journal of Organic Chemistry, 1996
- The Aldol Reaction: Acid and General Base CatalysisPublished by Elsevier ,1991
- Novel synthesis of β-siloxy esters by condensation of carbonyls and trimethylsilane with α,β-unsaturated esters catalyzed by RhCl3Tetrahedron Letters, 1987
- Heterolytic Activation of Hydrogen by Transition Metal ComplexesPublished by Wiley ,1981
- Catalytic hydrogenation using cationic rhodium complexes. I. Evolution of the catalytic system and the hydrogenation of olefinsJournal of the American Chemical Society, 1976