Chiral ligands containing heteroatoms. 15.1 cyclic β-amino alcohols as chiral inductors for enantioselective reductions of ketones
Cristina Collu
Tetrahedron: Asymmetry, 1996
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A New Family of Modular Chiral Ligands for the Catalytic Enantioselective Reduction of Prochiral Ketones
Albert Moyano
The Journal of Organic Chemistry, 1999
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Novel Chiral Switching Ligands for Enantioselective Asymmetric Reductions of Prochiral Ketones
Sivan Velmathi
Molecules, 2001
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A comparative study of reactivity and selectivity of chiral diamines and structurally analogous amino alcohol ligands in enantioselective alkylations with diethylzinc
Antonio Rocha Gonsalves
Applied Organometallic Chemistry, 2008
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ChemInform Abstract: Amino Acid Ligand Chirality for Enantioselective Syntheses
Gyula Pályi
ChemInform, 2010
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Enantioselective reformatsky reaction induced by chiral β-amino alcohols
Rafael Pedrosa
Tetrahedron, 1997
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Renewable Chiral Auxiliary for Enantioselective Synthesis of α-aminoacids
Cristina Ott
revistadechimie.ro
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Enantioselective synthesis of secondary alcohols in the presence of chiral ligands
Lino Colombo
Tetrahedron, 1982
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Enantioselective reformatsky reaction induced by chiral �-amino alcohols
Rafael Pedrosa
Tetrahedron, 1997
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Chiral ligands containing heteroatoms. III. Enantioselective ketone reductions using tin(II) organometallic systems from chiral piperazines
mauro marchetti
Tetrahedron Letters, 1989
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New approach to exclusive formation of both enantiomers of β-amino acid derivatives
Ana Cardoso
Tetrahedron, 2008
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New approach to exclusive formation of both enantiomers of �-amino acid derivatives
Jesus De Los Santos
Tetrahedron, 2008
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Stereoselective synthesis of 1,3-amino alcohols and 1,3-amino ketones
Argimiro Lopez Viado
The Journal of Organic Chemistry, 1992
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ChemInform Abstract: Chiral Ligands Containing Heteroatoms. Part 7. An Investigation on the Stereochemistry of the Ketone Reductions by Chiral Diamines/Tin Hydride Systems
Cristina Collu
ChemInform, 2010
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Convenient Methods for the Synthesis of Chiral Amino Alcohols and Amines
Shaik Anwar
CHIMIA International Journal for Chemistry, 2013
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Chiral ligands containing heteroatoms.7. An investigation on the stereochemistry of the ketone reductions by chiral diamines/tin hydride systems
mauro marchetti
Tetrahedron: Asymmetry, 1991
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Amino acid chirons: a tool for asymmetric synthesis of heterocycles
Priyanka Singh
Organic & biomolecular chemistry, 2014
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Stereoselective reduction of prochiral ketones, using aluminum hydride reagents prepared from lialh4 and chiral diethanolamines
Arne Van Der Gen
Tetrahedron: Asymmetry, 1994
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Synthesis of a Family of Fine-Tunable New Chiral Ligands for Catalytic Asymmetric Synthesis. Ligand Optimization through the Enantioselective Addition of Diethylzinc to Aldehydes
Albert Moyano
The Journal of Organic Chemistry, 1997
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Diastereoselective synthesis of enantioenriched homopropargyl amino alcohols from α-dibenzylamino aldehydes and their use as chiral synthons
Rafael Pedrosa
Tetrahedron, 2006
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Chiral enolate design
David Mathre
Pure and Applied Chemistry, 2000
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Enantioselective Generation and Diastereoselective Reactions of Chiral Enolates Derived from ?-Heterosubstituted Carboxylic Acids. Preliminary Communication
Reto Naef
Helvetica Chimica Acta, 1981
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N-Substituted Ephedrines as Chiral Auxiliaries in Enantioselective Alkylation Reactions of Carbonyl Compounds
Alejandro Cruz
Current Organic Synthesis, 2015
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A Regio- and Stereodivergent Route to All Isomers of v ic -Amino Alcohols
Berit Olofsson
The Journal of Organic Chemistry, 2002
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Chiral Amine Synthesis - Recent Developments and Trends for Enamide Reduction, Reductive Amination, and Imine Reduction
Mohamed Elshazly
Advanced Synthesis & Catalysis, 2010
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Synthesis and applications of secondary amine derivatives of (+)-dehydroabietylamine in chiral molecular recognition
Sami Heikkinen
Organic & Biomolecular Chemistry, 2015
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Enantioselective Synthesis, Enantiomeric Separations and Chiral Recognition
Madalena Pinto
Molecules, 2020
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The design, synthesis, and application of a chiral coupling reagent derived from strychnine for the enantioselective activation of a carboxylic group
Katarzyna Kasperowicz
Tetrahedron Letters, 2010
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Asymmetric syntheses with chiral oxazaborolidines
Jürgen Martens
Tetrahedron: Asymmetry, 1992
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