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Asymmetric catalysis in organic synthesis
Ryoji Noyori
- 01 Jan 1994
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TL;DR: In this article, the authors present a textbook of practical organic chemistry with Electronic Structure Methods (ESM) for HPLC and HPLC-based problem solving in organic synthesis.
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Abstract: General books Advanced organic chemistry March 5 ed Advanced practical organic chemistry Leonard, Lygo, Procter 2 ed Asymmetric catalysis in organic synthesis Noyori Chirotechnology Sheldon CRC Handbook of Chemistry and Physics Lide 86 ed Exploring Chemistry with Electronic Structure Methods Foresman, Frisch Modern allene chemistry vol 1 Krause, Hashmi Modern allene chemistry vol 2 Krause, Hashmi Modern oxidation methods Bäckvall Organic chemistry Solomons 6 ed Practical Problem Solving in HPLC Kromidas Protective groups in organic synthesis Greene 3 ed Purification of laboratory chemicals Armarego, Chai 5 ed Textbook of practical organic chemistry Vogel 4 ed
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Citations
Preparation of new chiral pyridine–phosphine ligands and their Pd-catalyzed asymmetric allylic alkylations
Jun'ichi Uenishi,Masahiro Hamada +1 more
TL;DR: In this article, an asymmetric allylic alkylation of 1,3-diphenyl-2-propenyl acetate with dimethyl malonate sodium salt using the (S,S)-ligand was presented.
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Enantioselective synthesis of 1,1,1-trifluoroalkan-2-ols by ruthenium-catalyzed hydrogenation
TL;DR: In this article, the highly enantioselective synthesis of 1,1,1-trifluoroalkan-2-ols has been achieved by hydrogenating enol acetates in the presence of chiral ruthenium catalysts.
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Hydroxyamide-Based Ligands and Their Use in the Asymmetric Catalysis of Key Organic Transformations
Paul Geoghegan,Patrick O'Leary +1 more
TL;DR: Asymmetric ligands whose key functional component consists of an amide and hydroxyl functional groups, in the absence of other co-ordinating groups, are a relatively recent development in asymmetric catalysis as discussed by the authors.
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Effects of ring substituents on enantioselective recognition of amino alcohols and acids in uryl-based binol receptors
TL;DR: In this paper, the effects of ring substituents on the stereoselective recognition of amino alcohols, (substituted phenyl)uryl-based chiral binol receptors have been prepared.
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Axial 4,4',6,6'-tetrakis-trifluoromethyl-biphenyl-2,2'-diamine (TF-BIPHAM): resolution and applications in asymmetric hydrogenation.
TL;DR: The racemic TF-BIPHAM was resolved for the first time, and the effectiveness of the resolved diamine was demonstrated by highly enantioselective hydrogenation of alpha-aryl enamides and alpha-dehydroamino acid esters using readily accessible bis(aminophosphine) ligands.
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