Chalcogen bond-guided conformational isomerization enables catalytic dynamic kinetic resolution of sulfoxides
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2041-1723
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Chalcogen bond-guided conformational isomerization enables catalytic dynamic kinetic resolution of sulfoxides ; volume:13 ; number:1 ; day:15 ; month:8 ; year:2022 ; pages:1-8 ; date:12.2022
Nature Communications ; 13, Heft 1 (15.8.2022), 1-8, 12.2022
- Urheber
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1038/s41467-022-32428-4
- URN
-
urn:nbn:de:101:1-2022110220253616488760
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:28 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Liu, Jianjian
- Zhou, Mali
- Deng, Rui
- Zheng, Pengcheng
- Chi, Yonggui Robin
- SpringerLink (Online service)
Ähnliche Objekte (12)
Selection of isomerization pathways of multistep photoswitches by chalcogen bonding
Membrane Environment Enables Ultrafast Isomerization of Amphiphilic Azobenzene
Thermodynamic Control Enables trans-Selective Isomerization of Vicinal Diols via Iridium Photocatalysis
Heteroalkyl‐Substitution in Molecular Organic Semiconductors: Chalcogen Effect on Crystallography, Conformational Lock, and Charge Transport
The Nature of Strong Chalcogen Bonds Involving Chalcogen‐Containing Heterocycles
Exploiting π and Chalcogen Interactions for the β‐Selective Glycosylation of Indoles through Glycal Conformational Distortion
Exploiting π and Chalcogen Interactions for the β‐Selective Glycosylation of Indoles through Glycal Conformational Distortion
Kinetic Salt Effect on Base‐Catalyzed Isomerization of d ‐Glucose into d ‐Fructose
i-shaped antibody engineering enables conformational tuning of biotherapeutic receptor agonists
Kinetic barriers in the isomerization of substituted ureas: implications for computer-aided drug design
Chalcogen based organocatalysts in transesterification
Thermoplasmonic Effect Enables Indirect ON–OFF Control over the Z‐E Isomerization of Azobenzene‐Based Photoswitch
Selection of isomerization pathways of multistep photoswitches by chalcogen bonding
Membrane Environment Enables Ultrafast Isomerization of Amphiphilic Azobenzene
Thermodynamic Control Enables trans-Selective Isomerization of Vicinal Diols via Iridium Photocatalysis
Heteroalkyl‐Substitution in Molecular Organic Semiconductors: Chalcogen Effect on Crystallography, Conformational Lock, and Charge Transport
The Nature of Strong Chalcogen Bonds Involving Chalcogen‐Containing Heterocycles
Exploiting π and Chalcogen Interactions for the β‐Selective Glycosylation of Indoles through Glycal Conformational Distortion
Exploiting π and Chalcogen Interactions for the β‐Selective Glycosylation of Indoles through Glycal Conformational Distortion
Kinetic Salt Effect on Base‐Catalyzed Isomerization of d ‐Glucose into d ‐Fructose
i-shaped antibody engineering enables conformational tuning of biotherapeutic receptor agonists
Kinetic barriers in the isomerization of substituted ureas: implications for computer-aided drug design
Chalcogen based organocatalysts in transesterification
Thermoplasmonic Effect Enables Indirect ON–OFF Control over the Z‐E Isomerization of Azobenzene‐Based Photoswitch
Selection of isomerization pathways of multistep photoswitches by chalcogen bonding
Membrane Environment Enables Ultrafast Isomerization of Amphiphilic Azobenzene
Thermodynamic Control Enables trans-Selective Isomerization of Vicinal Diols via Iridium Photocatalysis
Heteroalkyl‐Substitution in Molecular Organic Semiconductors: Chalcogen Effect on Crystallography, Conformational Lock, and Charge Transport
The Nature of Strong Chalcogen Bonds Involving Chalcogen‐Containing Heterocycles
Exploiting π and Chalcogen Interactions for the β‐Selective Glycosylation of Indoles through Glycal Conformational Distortion
Exploiting π and Chalcogen Interactions for the β‐Selective Glycosylation of Indoles through Glycal Conformational Distortion
Kinetic Salt Effect on Base‐Catalyzed Isomerization of d ‐Glucose into d ‐Fructose
i-shaped antibody engineering enables conformational tuning of biotherapeutic receptor agonists
Kinetic barriers in the isomerization of substituted ureas: implications for computer-aided drug design
Chalcogen based organocatalysts in transesterification