Biological Stereoselectivity of Atropisomeric Natural Products and Drugs
about
Chiral recognition and atropisomerism in the sevoflurane dimer.Atropselective syntheses of (-) and (+) rugulotrosin A utilizing point-to-axial chirality transfer.Practical Organocatalytic Synthesis of Functionalized Non-C2-Symmetrical Atropisomeric Biaryls.Synthesis of enantiomerically pure helicene like bis-oxazines from atropisomeric 7,7'-dihydroxy BINOL: Preliminary measurements of the circularly polarized luminescence.SET-induced biaryl cross-coupling: an S(RN)1 reaction.Symmetry in Cascade Chirality-Transfer Processes: A Catalytic Atroposelective Direct Arylation Approach to BINOL Derivatives.The solid-state continuum: a perspective on the interrelationships between different solid-state forms in drug substance and drug product.A twist of nature--the significance of atropisomers in biological systems.Organocatalyzed Asymmetric Synthesis of Axially, Planar, and Helical Chiral Compounds.A microchip electrophoresis-mass spectrometric platform for fast separation and identification of enantiomers employing the partial filling technique.Exploiting Atropisomerism to Increase the Target Selectivity of Kinase Inhibitors.Atropisomerism in medicinal chemistry: challenges and opportunities.Catalytic enantioselective synthesis of atropisomeric biaryls by a cation-directed O-alkylation.Induction of Axial Chirality in 8-Arylquinolines through Halogenation Reactions Using Bifunctional Organocatalysts.Anion-π Catalysts with Axial Chirality.Ultraviolet-Visible Chiroptical Activity of Aluminum Nanostructures.General Enantioselective C-H Activation with Efficiently Tunable Cyclopentadienyl Ligands.Conformational Studies and Atropisomerism Kinetics of the ALK Clinical Candidate Lorlatinib (PF-06463922) and Desmethyl Congeners.Enantioselective syntheses of atropisomers featuring a five-membered ring.Chiral cobalt(ii) complex catalyzed Friedel-Crafts aromatization for the synthesis of axially chiral biaryldiols.Combining Organocatalysis with Central-to-Axial Chirality Conversion: Atroposelective Hantzsch-Type Synthesis of 4-Arylpyridines.Enantioselective Synthesis of Pyrrolopyrimidine Scaffolds through Cation-Directed Nucleophilic Aromatic Substitution.
P2860
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P2860
Biological Stereoselectivity of Atropisomeric Natural Products and Drugs
description
2013 nî lūn-bûn
@nan
2013 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Biological Stereoselectivity of Atropisomeric Natural Products and Drugs
@ast
Biological Stereoselectivity of Atropisomeric Natural Products and Drugs
@en
type
label
Biological Stereoselectivity of Atropisomeric Natural Products and Drugs
@ast
Biological Stereoselectivity of Atropisomeric Natural Products and Drugs
@en
prefLabel
Biological Stereoselectivity of Atropisomeric Natural Products and Drugs
@ast
Biological Stereoselectivity of Atropisomeric Natural Products and Drugs
@en
P2093
P2860
P356
P1433
P1476
Biological Stereoselectivity of Atropisomeric Natural Products and Drugs
@en
P2093
George A. Ellestad
John Murphy
P2860
P304
P356
10.1002/CHIR.22145
P577
2013-04-26T00:00:00Z