- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
In: 10.1055/s-0037-1610369
- Ereignis
-
Veröffentlichung
- (wo)
-
Aachen
- (wer)
-
Universitätsbibliothek der RWTH Aachen
- (wann)
-
2018
- Urheber
- DOI
-
10.18154/RWTH-2019-00215
- URN
-
urn:nbn:de:101:1-2019082206330379311921
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:56 MEZ
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
- Wang, Han
- Zhang, Duo
- Cao, Mengwei
- Bolm, Carsten
- Universitätsbibliothek der RWTH Aachen
Entstanden
- 2018
Ähnliche Objekte (12)
NH-functionalization of sulfoximines by using hypervalent iodine reagents
Applications of hypervalent iodine(III) reagents in sulfoximidations
Chirale Katalysatoren für enantioselektive C-C-Verknüpfungen
Activating unreactive substrates : the role of secondary interactions
Valorization of lignin by employing solution chemistry and mechanochemical conditions
[Cp*RhCl 2 ] 2 : mechanosynthesis and applications in C–H bond functionalisations under ball-milling conditions
Method development for the synthesis of organosulfur compounds and their functionalization by C–H activation and reductive borylation
Base-mediated defluorinative alkylations of NH/N-acyl sulfoximines and conversions of N-methyl S, S-diaryl sulfoximines by S=N/S–C bond cleavage reactions
Photoinduced acylations of sulfoximines and transformations of an N-phthalimidoyl sulfoximine
Selective transformations of sulfondiimines
Syntheses of sulfoximines : development of a light-promoted protocol and its application in the preparation of natural compound analogs
Functionalization of Sulfur-Nitrogen compounds and the synthesis of an allicin analogue
NH-functionalization of sulfoximines by using hypervalent iodine reagents
Applications of hypervalent iodine(III) reagents in sulfoximidations
Chirale Katalysatoren für enantioselektive C-C-Verknüpfungen
Activating unreactive substrates : the role of secondary interactions
Valorization of lignin by employing solution chemistry and mechanochemical conditions
[Cp*RhCl 2 ] 2 : mechanosynthesis and applications in C–H bond functionalisations under ball-milling conditions
Method development for the synthesis of organosulfur compounds and their functionalization by C–H activation and reductive borylation
Base-mediated defluorinative alkylations of NH/N-acyl sulfoximines and conversions of N-methyl S, S-diaryl sulfoximines by S=N/S–C bond cleavage reactions
Photoinduced acylations of sulfoximines and transformations of an N-phthalimidoyl sulfoximine
Selective transformations of sulfondiimines
Syntheses of sulfoximines : development of a light-promoted protocol and its application in the preparation of natural compound analogs
Functionalization of Sulfur-Nitrogen compounds and the synthesis of an allicin analogue
NH-functionalization of sulfoximines by using hypervalent iodine reagents
Applications of hypervalent iodine(III) reagents in sulfoximidations
Chirale Katalysatoren für enantioselektive C-C-Verknüpfungen
Activating unreactive substrates : the role of secondary interactions
Valorization of lignin by employing solution chemistry and mechanochemical conditions
[Cp*RhCl 2 ] 2 : mechanosynthesis and applications in C–H bond functionalisations under ball-milling conditions
Method development for the synthesis of organosulfur compounds and their functionalization by C–H activation and reductive borylation
Base-mediated defluorinative alkylations of NH/N-acyl sulfoximines and conversions of N-methyl S, S-diaryl sulfoximines by S=N/S–C bond cleavage reactions
Photoinduced acylations of sulfoximines and transformations of an N-phthalimidoyl sulfoximine
Selective transformations of sulfondiimines
Syntheses of sulfoximines : development of a light-promoted protocol and its application in the preparation of natural compound analogs