Related references
Note: Only part of the references are listed.Selenide Ions as Catalysts for Homo- and Crossed-Tishchenko Reactions of Expanded Scope
Simon P. Curran et al.
ORGANIC LETTERS (2012)
Selective Crossed-Tishchenko Reaction-A Waste-Free Synthesis of Benzyl Esters
Wojciech I. Dzik et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2011)
Bicyclic guanidinate compounds of magnesium and their activity as pre-catalysts in the Tishchenko reaction
Benjamin M. Day et al.
CHEMICAL COMMUNICATIONS (2011)
Highly Chemoselective Direct Crossed Aliphatic-Aromatic Acyloin Condensations with Triazolium-Derived Carbene Catalysts
Sarah E. O'Toole et al.
JOURNAL OF ORGANIC CHEMISTRY (2011)
Nickel-Catalyzed Selective Conversion of Two Different Aldehydes to Cross-Coupled Esters
Yoichi Hoshimoto et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2011)
Microwave-assisted efficient thiolate-catalysed homo- and crossed intermolecular Tishchenko reactions
Cornelius J. O' Connor et al.
NEW JOURNAL OF CHEMISTRY (2011)
Tunable Bromomagnesium Thiolate Tishchenko Reaction Catalysts: Intermolecular Aldehyde-Trifluoromethylketone Coupling
Linda Cronin et al.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2010)
Nickel-catalyzed Tishchenko reaction via hetero-nickelacycles by oxidative cyclization of aldehydes with nickel(0) complex
Sensuke Ogoshi et al.
CHEMICAL COMMUNICATIONS (2010)
Sodium Hydride Catalyzed Tishchenko Reaction
Thomas Werner et al.
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2010)
An environmentally benign solvent-free Tishchenko reaction
Daniel C. Waddell et al.
GREEN CHEMISTRY (2009)
Organoactinides promote the Tishchenko reaction: The myth of inactive actinide-alkoxo complexes
Tamer Andrea et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2008)
Lithium bromide as a flexible, mild, and recyclable reagent for solvent-free Cannizzaro, Tishchenko, and Meerwein-Ponndorf-Verley reactions
Mohammad M. Mojtahedi et al.
ORGANIC LETTERS (2007)
Heavier alkaline earth amides as catalysts for the Tischenko reaction
Mark R. Crimmin et al.
ORGANIC LETTERS (2007)
The Tishchenko reaction: A classic and practical tool for ester synthesis
Tsunetake Seki et al.
CHEMISTRY LETTERS (2006)
Hydroacylation of activated ketones catalyzed by N-heterocyclic carbenes
A Chan et al.
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2006)
The first crystal structure of a thioacylenzyme intermediate in the ALDH family: New coenzyme conformation and relevance to catalysis
K D'Ambrosio et al.
BIOCHEMISTRY (2006)
Tishchenko reaction using an iridium-ligand bifunctional catalyst
T Suzuki et al.
SYNLETT (2005)
Tishchenko reactions and Oppenauer oxidation reactions of aldehydes promoted by diisobutylaluminum hydride
YS Hon et al.
TETRAHEDRON LETTERS (2004)
Reactions of a hexahydride-osmium complex with aldehydes:: Double C-Hα activation-decarbonylation and single C-Hα activation-hydroxylation tandem processes and catalytic Tishchenko reactions
P Barrio et al.
ORGANOMETALLICS (2004)
Isopropoxyaluminum 1,1′-biphenyl-2-oxy-2′-perfluorooctanesulfonamide as a catalyst for Tishchenko reaction
T Ooi et al.
TETRAHEDRON LETTERS (2003)
Stereoselective synthesis of δ-lactones from 5-oxoalkanals via one-pot sequential acetalization, tishchenko reaction, and lactonization by cooperative catalysis of samarium ion and mercaptan
JL Hsu et al.
JOURNAL OF ORGANIC CHEMISTRY (2001)
Share Paper
