- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Direct Amination of Alkyl and Aryl Pinacol Boronates ; volume:9 ; number:01 ; year:2012 ; pages:0086-0086
Synfacts ; 9, Heft 01 (2012), 0086-0086
- DOI
-
10.1055/s-0032-1317730
- URN
-
urn:nbn:de:101:1-2018090212271988867456
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:20 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Other Objects (12)
Direct Chan–Lam Amination and Etherification of Aryl BMIDA Reagents
N-Boc-O-Tosyl Hydroxylamine as a Safe and Efficient Nitrogen Source for the N-Amination of Aryl and Alkyl Amines: Electrophylic Amination
Catalysed Aryl Amine Syntheses via Azides: From Azidation of Aryl Halides to Azide Reduction and Direct Amination
Über Alkyl(aryl)mercapto-thiocarbonyl-thiocyanate und Alkyl(aryl)mercapto-thiocarbonyl-isothiocyanate
Iridium-catalyzed direct asymmetric reductive amination utilizing primary alkyl amines as the N-sources
Beiträge zur Chemie von 2-Alkyl(Aryl)-4,6-bis(alkyl(aryl)-thio)- 1,3,5-oxa(thia)diazinium-hexachloroantimonaten(V) [Alkyl-aryl-bis-alkyl-aryl-thio-oxa-thiadiazinium- hexachloroantimonaten]
Neue Heterocyclen aus 2-(α- Alkyl(aryl)aminobenzyl)-benzimidazolen [Alpha-Alkyl(aryl)aminobenzyl-benzimidazolen]
Beiträge zur Chemie der 5-Alkyl(aryl)imino-2-alkyl(aryl)- 3-aryl-Δ3-1,2,4-thiadiazoline
Zur Kenntnis basischer Aryl-alkyl-äther
General Synthesis of Alkyl Amines via Borrowing Hydrogen and Reductive Amination
General Synthesis of Alkyl Amines via Borrowing Hydrogen and Reductive Amination
Nucleophilic Amination of Aryl Halides with an Azanide Surrogate
Direct Chan–Lam Amination and Etherification of Aryl BMIDA Reagents
N-Boc-O-Tosyl Hydroxylamine as a Safe and Efficient Nitrogen Source for the N-Amination of Aryl and Alkyl Amines: Electrophylic Amination
Catalysed Aryl Amine Syntheses via Azides: From Azidation of Aryl Halides to Azide Reduction and Direct Amination
Über Alkyl(aryl)mercapto-thiocarbonyl-thiocyanate und Alkyl(aryl)mercapto-thiocarbonyl-isothiocyanate
Iridium-catalyzed direct asymmetric reductive amination utilizing primary alkyl amines as the N-sources
Beiträge zur Chemie von 2-Alkyl(Aryl)-4,6-bis(alkyl(aryl)-thio)- 1,3,5-oxa(thia)diazinium-hexachloroantimonaten(V) [Alkyl-aryl-bis-alkyl-aryl-thio-oxa-thiadiazinium- hexachloroantimonaten]
Neue Heterocyclen aus 2-(α- Alkyl(aryl)aminobenzyl)-benzimidazolen [Alpha-Alkyl(aryl)aminobenzyl-benzimidazolen]
Beiträge zur Chemie der 5-Alkyl(aryl)imino-2-alkyl(aryl)- 3-aryl-Δ3-1,2,4-thiadiazoline
Zur Kenntnis basischer Aryl-alkyl-äther
General Synthesis of Alkyl Amines via Borrowing Hydrogen and Reductive Amination
General Synthesis of Alkyl Amines via Borrowing Hydrogen and Reductive Amination
Nucleophilic Amination of Aryl Halides with an Azanide Surrogate
Direct Chan–Lam Amination and Etherification of Aryl BMIDA Reagents
N-Boc-O-Tosyl Hydroxylamine as a Safe and Efficient Nitrogen Source for the N-Amination of Aryl and Alkyl Amines: Electrophylic Amination
Catalysed Aryl Amine Syntheses via Azides: From Azidation of Aryl Halides to Azide Reduction and Direct Amination
Über Alkyl(aryl)mercapto-thiocarbonyl-thiocyanate und Alkyl(aryl)mercapto-thiocarbonyl-isothiocyanate
Iridium-catalyzed direct asymmetric reductive amination utilizing primary alkyl amines as the N-sources
Beiträge zur Chemie von 2-Alkyl(Aryl)-4,6-bis(alkyl(aryl)-thio)- 1,3,5-oxa(thia)diazinium-hexachloroantimonaten(V) [Alkyl-aryl-bis-alkyl-aryl-thio-oxa-thiadiazinium- hexachloroantimonaten]
Neue Heterocyclen aus 2-(α- Alkyl(aryl)aminobenzyl)-benzimidazolen [Alpha-Alkyl(aryl)aminobenzyl-benzimidazolen]
Beiträge zur Chemie der 5-Alkyl(aryl)imino-2-alkyl(aryl)- 3-aryl-Δ3-1,2,4-thiadiazoline
Zur Kenntnis basischer Aryl-alkyl-äther
General Synthesis of Alkyl Amines via Borrowing Hydrogen and Reductive Amination
General Synthesis of Alkyl Amines via Borrowing Hydrogen and Reductive Amination