about
Reversible bond formation enables the replication and amplification of a crosslinking salen complex as an orthogonal base pairCarbohydrates as enantioinduction components in stereoselective catalysisChemistry. Heat and light switch a chiral catalyst and its productsTandem synthesis of alternating polyesters from renewable resourcesAspartyl Oxidation Catalysts That Dial In Functional Group Selectivity, along with Regio- and StereoselectivityCombining a Clostridial enzyme exhibiting unusual active site plasticity with a remarkably facile sigmatropic rearrangement: rapid, stereocontrolled entry into densely functionalized fluorinated phosphonates for chemical biologyNMR spectroscopic detection of chirality and enantiopurity in referenced systems without formation of diastereomersOrganoselenium ligands in catalysis.Cooperative expression of atomic chirality in inorganic nanostructures.Enantioselective addition of boronates to acyl imines catalyzed by chiral biphenols.Assessment of the various ionization methods in the analysis of metal salen complexes by mass spectrometry.Enantioselectivity in environmental safety of current chiral insecticides.Adaptation of a small-molecule hydrogen-bond donor catalyst to an enantioselective hetero-Diels-Alder reaction hypothesized for brevianamide biosynthesis.The Mannich reaction of malonates with simple imines catalyzed by bifunctional cinchona alkaloids: enantioselective synthesis of beta-amino acids.Dimeric Cinchona alkaloidsModular solid-phase synthesis, catalytic application and efficient recycling of supported phosphine-phosphite ligand libraries.TADDOL-based phosphorus(III)-ligands in enantioselective Pd(0)-catalysed C-H functionalisations.Chiral N-heterocyclic carbenes as stereodirecting ligands in asymmetric catalysis.Adaptable P-X Biaryl Phosphite/Phosphoroamidite-Containing Ligands for Asymmetric Hydrogenation and C-X Bond-Forming Reactions: Ligand Libraries with Exceptionally Wide Substrate Scope.Asymmetry on large scale: the roadmap to stereoselective processes.A Synergistic Combinatorial and Chiroptical Study of Peptide Catalysts for Asymmetric Baeyer-Villiger Oxidation.Diametric stereocontrol in dynamic catalytic reduction of racemic acyl phosphonates: divergence from α-keto ester congenersHydroxamic acids in asymmetric synthesis.Structural revisions of small molecules reported to cross-link G-quadruplex DNA in vivo reveal a repetitive assignment error in the literatureStructural studies of β-turn-containing peptide catalysts for atroposelective quinazolinone bromination.A green chemistry approach to asymmetric catalysis: solvent-free and highly concentrated reactionsNew chemistry with old functional groups: on the reaction of isonitriles with carboxylic acids--a route to various amide types.Investigation of a Privileged Polymorphic Motif: a Dimeric ROY Derivative.Asymmetric catalysis at a distance: catalytic, site-selective phosphorylation of teicoplaninNatural products as inspiration for the development of asymmetric catalysis.Revisiting the modularity of modular polyketide synthases.Diversity of Secondary Structure in Catalytic Peptides with β-Turn-Biased SequencesDesign of chiral ligands for asymmetric catalysis: from C2-symmetric P,P- and N,N-ligands to sterically and electronically nonsymmetrical P,N-ligandsDevelopment and applications of tethered bis(8-quinolinolato) metal complexes (TBOxM).Asymmetric catalysis with chiral oxazolidine ligands.Recent advances in enantioselective organocatalyzed anhydride desymmetrization and its application to the synthesis of valuable enantiopure compounds.Fluorine conformational effects in organocatalysis: an emerging strategy for molecular design.Cinchona-based primary amine catalysis in the asymmetric functionalization of carbonyl compounds.Catalytic selective synthesis.Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate.
P2860
Q27674400-8D8EB53C-C108-446C-B174-24C41D87D1CEQ28072011-0445FE47-02C5-4A23-8E05-9A81269F8429Q28307584-BCF0F79E-DC48-465B-BE13-4D3465132AD8Q28740709-A4C66B1A-B051-4B0D-8276-65F930416A63Q28820785-3894E05B-D4A1-488D-814B-4BB04E382094Q28833210-D9AE6A0E-E67B-4B9F-AACD-1B65F9FBC685Q30543897-09C27AAE-432D-409E-BB2B-88185975B366Q30558521-DAAB8BC1-D48C-4EEB-B11D-562753120E9EQ30837877-5BC25AA6-4478-4572-84E2-17E093AF9EA8Q33442924-48E9878B-00B4-43B2-A30B-A6100309812AQ33461565-12E0D145-DD17-46FE-91D5-D38A163B3EA4Q33756966-FEF85EBA-4E7B-42CB-83B8-9F5FCFDB9B09Q35119989-7BF127A9-FACA-46BC-BCB8-F6B2731CCEE9Q35210367-62DA6059-8157-4152-9934-4C1700DD6166Q35546281-F53269E8-39E8-41D5-BA42-D566E577BA47Q35815239-86A0F329-DAF9-4E90-9BDF-2670FA8AB465Q35825220-3C658C9D-DA85-4A53-AA46-7BB60C9B4BDDQ35981088-6EC91304-7674-4DA2-B646-DA459582B693Q36057224-53A4066C-7D8D-408F-88C4-DA6EC82B2075Q36205821-8458F2B3-136B-45B2-9888-0A5177B130B8Q36239717-52AB6450-9F5E-4D76-832B-AB7628FBB95AQ36554768-3691B674-0A37-4874-B921-3880DFF72DEDQ36625454-C0E61D03-F535-4E4F-8585-C8EE5D763782Q36719551-284B2897-044D-4C12-826A-147F9852764CQ36734244-33D954E4-B995-42CE-9D13-7E3C15538BCAQ36851982-8574FF5E-FF9A-4DED-A540-B27BF6E214A7Q36967310-C2FA3ECD-C89B-468C-B25B-5A15AA7856EEQ37157332-F360155B-607D-4C59-A3EE-4FB9C0F273DAQ37215640-308995C5-AA41-44B8-8E7D-8840478512CCQ37272545-F219D288-7D69-4EE3-B5B2-242816141647Q37393154-5BAFFFE5-2C1A-479A-A783-40B614144FDBQ37646524-E01C588B-3C2E-4D8F-9B8B-EEFEBA3B286DQ37648743-F3D7666A-E5E4-4CC9-A8F5-0C218DCF981AQ37659921-FCE5EDF6-ADC7-4933-AF05-862CBBDF2121Q37829921-E81AE3E9-5EC3-4DB5-BFFF-DCE0E2D9F3E4Q37898012-DC1AB617-DD3D-47D4-AC3F-048C60A82C15Q37939749-45EF936F-D9FF-404E-89E8-9B0C17254A5EQ38034730-1D5D0212-48DD-443E-A769-910A430CFE77Q38046517-E126B0D4-C821-4A0E-8B30-80B7890F0460Q38097103-F6C640D2-B0A4-46DE-A74E-AD51872CDF47
P2860
description
2003 nî lūn-bûn
@nan
2003 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2003 թվականի մարտին հրատարակված գիտական հոդված
@hy
2003年の論文
@ja
2003年論文
@yue
2003年論文
@zh-hant
2003年論文
@zh-hk
2003年論文
@zh-mo
2003年論文
@zh-tw
2003年论文
@wuu
name
Privileged chiral catalysts.
@ast
Privileged chiral catalysts.
@en
Privileged chiral catalysts.
@nl
type
label
Privileged chiral catalysts.
@ast
Privileged chiral catalysts.
@en
Privileged chiral catalysts.
@nl
prefLabel
Privileged chiral catalysts.
@ast
Privileged chiral catalysts.
@en
Privileged chiral catalysts.
@nl
P356
P1433
P1476
Privileged chiral catalysts.
@en
P2093
Eric N Jacobsen
Tehshik P Yoon
P304
P356
10.1126/SCIENCE.1083622
P407
P577
2003-03-01T00:00:00Z