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Zhou Li.
Evolution of chiral Lewis basic N-formamide as highly effective organocatalyst for asymmetric reduction of both ketones and ketimines with an unprecedented substrate scope
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Chemical Communications, 2007
[DOI: 10.1039/b703307a]
Balaban, T. S.; Balaban, A. T., Science of Synthesis, (2003) 14, 82..
From Methyl(ene) Ketones and α,β-Unsaturated Ketones Followed by Dehydrocyclization
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Science of Synthesis
Takacs, J. M.; Vayalakkada, S., Science of Synthesis, (2001) 1, 327..
The Wacker Oxidation Using a Fluorous Biphasic System
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Science of Synthesis
Loren, Jon C.; Sharpless, K. Barry, Synthesis 2005, 1514-1520.
The Banert Cascade: A Synthetic Sequence to Polyfunctional NH-1,2,3-Triazoles
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Synthesis
[DOI: 10.1055/s-2005-869892]
Mostefaï, Naouël; Sirol, Sabine; Courmarcel, James; Riant, Olivier, Synthesis 2007, 1265-1271.
Air-Accelerated Enantioselective Hydrosilylation of Ketones Catalyzed by Copper(I) Fluoride&endash;Diphosphine Complexes: Investigations of the Effects of Temperature and Ligand Structure
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Synthesis
[DOI: 10.1055/s-2007-966000]
Cheemala, Murthy N.; Gayral, Maud; Brown, John M.; Rossen, Kai; Knochel, Paul, Synthesis 2007, 3877-3885.
New Paracyclophane Phosphine for Highly Enantioselective Ruthenium-Catalyzed Hydrogenation of Prochiral Ketones
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Synthesis
[DOI: 10.1055/s-2007-990917]
Alonso, Francisco; Riente, Paola; Yus, Miguel, Synlett 2007, 1877-1880.
The α-Alkylation of Methyl Ketones with Primary Alcohols Promoted by &linebreak;Nickel Nanoparticles under Mild and Ligandless Conditions
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Synlett
[DOI: 10.1055/s-2007-984522]
Cox, L. R., Science of Synthesis, (2008) 36, 134..
Biocatalytic Reduction Methods
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Science of Synthesis
Gosmini, C.; Corpet, M., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 1, 711..
Cobalt-Catalyzed Cross-Coupling Reactions of Arylzinc Species with Carboxylic Anhydrides
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Science of Synthesis
Liu, S.; Xiao, J., Science of Synthesis: Cross Coupling and Heck-Type Reactions, (2012) 3, 226..
With Aryl Halides in Alcohols
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Science of Synthesis
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