- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
Iodine(III)‐Based Halogen Bond Donors: Properties and Applications ; day:18 ; month:06 ; year:2021 ; extent:1
The chemical record ; (18.06.2021) (gesamt 1)
- Urheber
- DOI
-
10.1002/tcr.202100119
- URN
-
urn:nbn:de:101:1-2021062317125575686834
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:50 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
- Robidas, Raphaël
- Reinhard, Dominik L.
- Legault, Claude Y.
- Huber, Stefan M.
Ähnliche Objekte (12)
Iodine(III)-based halogen bond donors : Properties and applications
Evaluation of 6‐Halogenated 2‐Pyridone Moieties as Halogen Bond Donors
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors
Evaluation of 6-halogenated 2-pyridone moieties as halogen bond donors
Bidentate Chiral Bis (imidazolium)‐Based Halogen‐Bond Donors: Synthesis and Applications in Enantioselective Recognition and Catalysis †
A bidentate iodine(III)-based halogen-bond donor as a powerful organocatalyst
Catalytic Carbon–Chlorine Bond Activation by Selenium‐Based Chalcogen Bond Donors
Activation of quinolines by cationic chalcogen bond donors
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors : Synthesis and applications in enantioselective recognition and catalysis
Polymer‐Bound Halogen Bonding Organocatalysis **
Nichtkovalente Organokatalyse mit Halogen‐, Chalkogen‐, Pniktogen‐ und Tetrelbrücken: neuere Entwicklungen
Halogen, Chalcogen, Pnictogen, and Tetrel Bonding in Non‐Covalent Organocatalysis: An Update
Iodine(III)-based halogen bond donors : Properties and applications
Evaluation of 6‐Halogenated 2‐Pyridone Moieties as Halogen Bond Donors
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors
Evaluation of 6-halogenated 2-pyridone moieties as halogen bond donors
Bidentate Chiral Bis (imidazolium)‐Based Halogen‐Bond Donors: Synthesis and Applications in Enantioselective Recognition and Catalysis †
A bidentate iodine(III)-based halogen-bond donor as a powerful organocatalyst
Catalytic Carbon–Chlorine Bond Activation by Selenium‐Based Chalcogen Bond Donors
Activation of quinolines by cationic chalcogen bond donors
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors : Synthesis and applications in enantioselective recognition and catalysis
Polymer‐Bound Halogen Bonding Organocatalysis **
Nichtkovalente Organokatalyse mit Halogen‐, Chalkogen‐, Pniktogen‐ und Tetrelbrücken: neuere Entwicklungen
Halogen, Chalcogen, Pnictogen, and Tetrel Bonding in Non‐Covalent Organocatalysis: An Update
Iodine(III)-based halogen bond donors : Properties and applications
Evaluation of 6‐Halogenated 2‐Pyridone Moieties as Halogen Bond Donors
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors
Evaluation of 6-halogenated 2-pyridone moieties as halogen bond donors
Bidentate Chiral Bis (imidazolium)‐Based Halogen‐Bond Donors: Synthesis and Applications in Enantioselective Recognition and Catalysis †
A bidentate iodine(III)-based halogen-bond donor as a powerful organocatalyst
Catalytic Carbon–Chlorine Bond Activation by Selenium‐Based Chalcogen Bond Donors
Activation of quinolines by cationic chalcogen bond donors
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors : Synthesis and applications in enantioselective recognition and catalysis
Polymer‐Bound Halogen Bonding Organocatalysis **
Nichtkovalente Organokatalyse mit Halogen‐, Chalkogen‐, Pniktogen‐ und Tetrelbrücken: neuere Entwicklungen