Optically active
View article: Asymmetric synthesis of stereogenic-at-sulfur compounds via biocatalytic oxidation with Unspecific Peroxygenases
Asymmetric synthesis of stereogenic-at-sulfur compounds via biocatalytic oxidation with Unspecific Peroxygenases Open
Stereogenic-at-sulfur compounds are vitally important biologically active small molecules, with many drugs featuring chiral sulfur atoms. Methods for the asymmetric synthesis of sulfoxide centres are well established, but methods that prod…
View article: Helical Dispiroindeno[2,1‑<i>c</i>]fluorenes Possessing Planar Chirality: Synthesis and ChiropticalProperties
Helical Dispiroindeno[2,1‑<i>c</i>]fluorenes Possessing Planar Chirality: Synthesis and ChiropticalProperties Open
Syntheses of enantioenriched helical dispiroindeno[2,1-c]fluorenes (DSIF) possessing one or two pCp moieties are presented. These are based on the conversion of (Sp)- and (Rp) pCp-carbaldehydes …
View article: Design of Phosphine-HeteroarenesulfonamideLigandsas Dinuclear Silver Catalysts for Enantioselective Construction ofα,β-Diamino Acids
Design of Phosphine-HeteroarenesulfonamideLigandsas Dinuclear Silver Catalysts for Enantioselective Construction ofα,β-Diamino Acids Open
We designed and developed a phosphine–heteroarenesulfonamide ligand and found that it functions as a chiral dinuclear silver catalyst capable of cooperatively activating both nucleophiles and electrophiles. As a result, a highly enantiosel…
View article: Results of Optically Stimulated Luminescence (OSL) dating.
Results of Optically Stimulated Luminescence (OSL) dating. Open
Results of Optically Stimulated Luminescence (OSL) dating.
View article: Iridium-Catalyzed EnantioselectiveC(<i>sp</i><sup>3</sup>)–H Borylation of Bicyclo[1.1.0]butanes
Iridium-Catalyzed EnantioselectiveC(<i>sp</i><sup>3</sup>)–H Borylation of Bicyclo[1.1.0]butanes Open
Bicyclo[1.1.0]butanes (BCBs) have attracted considerable interest in organic synthesis due to their versatile reactivity. However, the asymmetric synthesis of these strained systems remains a formidable challenge. We herein report an iridi…
View article: EnantioselectiveSynthesis of Boron-Stereogenic HeterocyclesEnabled by Asymmetric Nickel Catalysis
EnantioselectiveSynthesis of Boron-Stereogenic HeterocyclesEnabled by Asymmetric Nickel Catalysis Open
Despite the widespread utilization of organoboron compounds across various areas, the efficient construction of stable and enantioenriched boron-centered chiral molecules remains a persistent challenge. Here, we present a nickel-catalyzed …
View article: Organoiodine-CatalyzedDesymmetric Fluorolactonizationof α,α-Diallylcarboxylic Acids to Access α‑QuaternaryFluorinated Lactones
Organoiodine-CatalyzedDesymmetric Fluorolactonizationof α,α-Diallylcarboxylic Acids to Access α‑QuaternaryFluorinated Lactones Open
The discovery of convenient and efficient methodologies for preparing optically active organofluorine compounds has received much attention from the synthetic community. Herein, we report an organoiodine-catalyzed desymmetric fluorolactoni…
View article: Interaction summary of catechin with the 51KQ active site.
Interaction summary of catechin with the 51KQ active site. Open
Interaction summary of catechin with the 51KQ active site.
View article: Optically Active Micellar‐Cubic Liquid Crystals from Quasi‐Racemic Octahedral Metallomesogens
Optically Active Micellar‐Cubic Liquid Crystals from Quasi‐Racemic Octahedral Metallomesogens Open
View article: Data from: Organocatalytic enantioselective addition of 3-aryloxindoles to ethenesulfonyl fluoride
Data from: Organocatalytic enantioselective addition of 3-aryloxindoles to ethenesulfonyl fluoride Open
We report the synthesis of chiral sulfonyl fluorides bearing a carbon quaternary stereocenter. A commercially available organocatalyst (DHQD)2AQN enables the enantioselective addition of 3-substituted oxindoles to ethenesulfonyl fluoride (…
View article: Data from: Organocatalytic enantioselective addition of 3-aryloxindoles to ethenesulfonyl fluoride
Data from: Organocatalytic enantioselective addition of 3-aryloxindoles to ethenesulfonyl fluoride Open
We report the synthesis of chiral sulfonyl fluorides bearing a carbon quaternary stereocenter. A commercially available organocatalyst (DHQD)2AQN enables the enantioselective addition of 3-substituted oxindoles to ethenesulfonyl fluoride (…
View article: Wavelength-dependent cross section for optically stimulated luminescence in Y <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML" altimg="si58.svg" display="inline" id="d1e183"> <mml:msub> <mml:mrow/> <mml:mrow> <mml:mn>2</mml:mn> </mml:mrow> </mml:msub> </mml:math> SiO5:Ce
Wavelength-dependent cross section for optically stimulated luminescence in Y SiO5:Ce Open
View article: Chiral Bifunctional Photocatalysts with Aromatic Ketones as Photosensitizers
Chiral Bifunctional Photocatalysts with Aromatic Ketones as Photosensitizers Open
Because the biological activity of a molecule is directly linked to its three-dimensional configuration, the preparation of chiral compounds is a central discipline in synthetic organic chemistry. With the exploitation of photoredox cataly…
View article: Triple-helical aggregates of copper( <scp>i</scp> ) cyclic trinuclear complexes for circularly polarized luminescence
Triple-helical aggregates of copper( <span>i</span> ) cyclic trinuclear complexes for circularly polarized luminescence Open
Self-assembly of Cu( i ) complexes via enantiomeric helical stacking produces homochiral triple-helical aggregates, enabling a record high luminescence dissymmetry factor (| g lum | > 1 × 10 −2 ) for coinage metal complexes in the red-NIR …
View article: Helically oriented polymer thin films by polarized UV-assisted vapor deposition polymerization
Helically oriented polymer thin films by polarized UV-assisted vapor deposition polymerization Open
Helically oriented polymer thin films were prepared by polarized UV-assisted vapor deposition polymerization of achiral polyazomethine. Stepwise modulation of the UV polarization axis during deposition induced chiral ordering, as confirmed…
View article: Halogenated Alkoxythiophene Additives Enhance the Performance of Organic Photodetectors
Halogenated Alkoxythiophene Additives Enhance the Performance of Organic Photodetectors Open
Morphological optimization of the active layer is pivotal for achieving high‐performance organic photodetectors (OPDs). Capitalizing on the simplicity and efficacy of additive strategies, a series of halogenated alkoxythiophene derivatives…
View article: Double Lateral Flow Test System for Simultaneous Immunodetection of Enantiomeric Forms of Antibiotics: An Ofloxacin Case Study
Double Lateral Flow Test System for Simultaneous Immunodetection of Enantiomeric Forms of Antibiotics: An Ofloxacin Case Study Open
Antibiotic stereoisomers as components of medicines are typically characterized by different biological activities. Because pharmaceuticals can include a racemic mixture of stereoisomers, monitoring of all forms is required. One contaminan…
View article: Chiral SURMOFs for Vibrational Circular Dichroism: Multiscale Modeling and Experimental Insights
Chiral SURMOFs for Vibrational Circular Dichroism: Multiscale Modeling and Experimental Insights Open
Chiral surface‐anchored metal‐organic frameworks (SURMOFs) are emerging as versatile platforms for enantioselective separation, sensing, and the manipulation of circularly polarized light. To harness their full potential, predictive modeli…
View article: Organocatalytic Enantioselective Addition of 3-Aryloxindoles to Ethenesulfonyl Fluoride
Organocatalytic Enantioselective Addition of 3-Aryloxindoles to Ethenesulfonyl Fluoride Open
We report the synthesis of chiral sulfonyl fluorides bearing a carbon quaternary stereocenter. A commercially available organocatalyst (DHQD)2AQN enables the enantioselective addition of 3-substituted oxindoles to ethenesulfonyl…
View article: OrganocatalyticEnantioselective Addition of 3‑Aryloxindolesto Ethenesulfonyl Fluoride
OrganocatalyticEnantioselective Addition of 3‑Aryloxindolesto Ethenesulfonyl Fluoride Open
We report the synthesis of chiral sulfonyl fluorides bearing a carbon quaternary stereocenter. A commercially available organocatalyst (DHQD)2AQN enables the enantioselective addition of 3-substituted oxindoles to ethenesulfonyl…
View article: Chiral Bisammonium-DirectedLiving Crystallization-DrivenSelf-Assembly Toward the Preparation of Nanostructures with ControlledDimensions and Tunable Chiroptical Properties
Chiral Bisammonium-DirectedLiving Crystallization-DrivenSelf-Assembly Toward the Preparation of Nanostructures with ControlledDimensions and Tunable Chiroptical Properties Open
Polymer nanostructures with controlled morphology and tunable chiroptical activities of circular dichroism (CD) and circularly polarized luminescence (CPL), showing promising applications ranging from information encryption to display, hav…
View article: Ultra-rapid, pressureless, and optically instrumented manufacturing of high-performance ceramics
Ultra-rapid, pressureless, and optically instrumented manufacturing of high-performance ceramics Open
View article: Chiral Borane-CatalyzedAsymmetric Hydrosilylationof 2,3,3-Trisubstituted 3<i>H</i>‑Indoles
Chiral Borane-CatalyzedAsymmetric Hydrosilylationof 2,3,3-Trisubstituted 3<i>H</i>‑Indoles Open
An asymmetric Piers-type hydrosilylation of 2,3,3-trisubstituted 3H-indoles has been achieved for the first time using a chiral borane catalyst derived by the in situ hydroboration of a chiral monoalkene with HB(C6F5…
View article: Synthesis of Bulky α-Cationic Phosphines and Their Applications in π-Acid Catalysis
Synthesis of Bulky α-Cationic Phosphines and Their Applications in π-Acid Catalysis Open
We have developed a synthetic method for triazolium-based bulky α-cationic phosphines. The influence of the steric properties of these cationic phosphines on the catalytic activity in the platinum-catalyzed hydroarylation of propargyl ethe…
View article: Stereoselective Pudovik reaction of aldehydes, aldimines, and nitroalkenes with CAMDOL-derived H-phosphonate
Stereoselective Pudovik reaction of aldehydes, aldimines, and nitroalkenes with CAMDOL-derived H-phosphonate Open
View article: Superimposed structures of synthesized derivatives (3a − e) in active site of 4N1U.
Superimposed structures of synthesized derivatives (3a − e) in active site of 4N1U. Open
Superimposed structures of synthesized derivatives (3a − e) in active site of 4N1U.
View article: Bienzymatic Dynamic Kinetic Resolution of Secondary Alcohols by Esterification/Racemization in Water
Bienzymatic Dynamic Kinetic Resolution of Secondary Alcohols by Esterification/Racemization in Water Open
The deposited dataset includes: (i) free induction decay (FID) files, acquisition data, and processing parameters for the recorded 1H, 13C, and 19F NMR spectra for a set of compounds [(hetero)aryl-alk…
View article: N-Heterocyclic Carbene-Catalyzed Enantioselective Synthesis of Inherently Chiral Pillar[5]arenes
N-Heterocyclic Carbene-Catalyzed Enantioselective Synthesis of Inherently Chiral Pillar[5]arenes Open
The catalytic enantioselective synthesis of inherently chiral pillar[5]arene derivatives holds significant promise in materials science, chemical biology, and host-guest chemistry, which is attributable to their unique pillar-shaped archit…
View article: Circling crystal in chiral active matter with self-alignment
Circling crystal in chiral active matter with self-alignment Open
The uploaded data are in text format and correspond to the position, active force, velocity, and orientation of the particles.
View article: Data from: Organocatalytic enantioselective addition of 3-aryloxindoles to ethenesulfonyl fluoride
Data from: Organocatalytic enantioselective addition of 3-aryloxindoles to ethenesulfonyl fluoride Open
We report the synthesis of chiral sulfonyl fluorides bearing a carbon quaternary stereocenter. A commercially available organocatalyst (DHQD)2AQN enables the enantioselective addition of 3-substituted oxindoles to ethenesulfonyl fluoride (…