Hochschulschrift
Imidazolium-based and related multidentate halogen-bond donors : synthesis, characterization and application in substitution and Diels-Alder reactions
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISBN
-
9783843911849
3843911843
- Maße
-
21 m, 316 g
- Umfang
-
173 S.
- Ausgabe
-
1. Aufl.
- Sprache
-
Englisch
- Anmerkungen
-
Ill., graph. Darst.
Zugl.: München, Techn. Univ. München, Diss., 2013
- Schlagwort
-
Imidazoliumsalze
Halogenorganische Verbindungen
Substitutionsreaktion
Diels-Alder-Reaktion
Chemische Reaktion
- Ereignis
-
Veröffentlichung
- (wo)
-
München
- (wer)
-
Verl. Dr. Hut
- (wann)
-
2013
- Urheber
- Inhaltsverzeichnis
- Rechteinformation
-
Bei diesem Objekt liegt nur das Inhaltsverzeichnis digital vor. Der Zugriff darauf ist unbeschränkt möglich.
- Letzte Aktualisierung
-
11.06.2025, 14:27 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.
Objekttyp
- Hochschulschrift
Beteiligte
- Walter, Sebastian Michael
- Verl. Dr. Hut
Entstanden
- 2013
Ähnliche Objekte (12)
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors : Synthesis and applications in enantioselective recognition and catalysis
Bidentate Chiral Bis (imidazolium)‐Based Halogen‐Bond Donors: Synthesis and Applications in Enantioselective Recognition and Catalysis †
Iodine(III)‐Based Halogen Bond Donors: Properties and Applications
Iodine(III)-based halogen bond donors : Properties and applications
Application of multidentate halogen-bond donors in organocatalysis and recognition
Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors
Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors
Halodifluoromethyl Moieties as Unconventional Halogen Bond Donors in Drug Discovery and Peptide Design
Crystal engineering with multipoint halogen bonding : double two‐point donors and acceptors at work
Crystal Engineering with Multipoint Halogen Bonding: Double Two‐Point Donors and Acceptors at Work
A comparison of structure, bonding and non-covalent interactions of aryl halide and diarylhalonium halogen-bond donors
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors : Synthesis and applications in enantioselective recognition and catalysis
Bidentate Chiral Bis (imidazolium)‐Based Halogen‐Bond Donors: Synthesis and Applications in Enantioselective Recognition and Catalysis †
Iodine(III)‐Based Halogen Bond Donors: Properties and Applications
Iodine(III)-based halogen bond donors : Properties and applications
Application of multidentate halogen-bond donors in organocatalysis and recognition
Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors
Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors
Halodifluoromethyl Moieties as Unconventional Halogen Bond Donors in Drug Discovery and Peptide Design
Crystal engineering with multipoint halogen bonding : double two‐point donors and acceptors at work
Crystal Engineering with Multipoint Halogen Bonding: Double Two‐Point Donors and Acceptors at Work
A comparison of structure, bonding and non-covalent interactions of aryl halide and diarylhalonium halogen-bond donors
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors
Bidentate chiral bis(imidazolium)‐based halogen‐bond donors : Synthesis and applications in enantioselective recognition and catalysis
Bidentate Chiral Bis (imidazolium)‐Based Halogen‐Bond Donors: Synthesis and Applications in Enantioselective Recognition and Catalysis †
Iodine(III)‐Based Halogen Bond Donors: Properties and Applications
Iodine(III)-based halogen bond donors : Properties and applications
Application of multidentate halogen-bond donors in organocatalysis and recognition
Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors
Carbonyl Hypoiodites as Extremely Strong Halogen Bond Donors
Halodifluoromethyl Moieties as Unconventional Halogen Bond Donors in Drug Discovery and Peptide Design
Crystal engineering with multipoint halogen bonding : double two‐point donors and acceptors at work
Crystal Engineering with Multipoint Halogen Bonding: Double Two‐Point Donors and Acceptors at Work