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Palladium/nickel-mediated cross coupling reaction between phosphorylamides and alkenes toward enephosphorylamides.
- Source :
-
Synthetic Communications . 2020, Vol. 50 Issue 15, p2338-2346. 9p. 1 Diagram, 3 Charts. - Publication Year :
- 2020
-
Abstract
- Enephosphorylamides were herein successfully prepared from phosphorylamides and substituted alkenes. The dehydrogenative transformation took place in the presence of a combination of a palladium diacetate and nickel dichloride. The transition metal-catalyzed methodology enjoyed high efficiency and broad substrate scope. Moreover, a plausible mechanism was proposed for the oxidative C–N cross coupling protocol. [ABSTRACT FROM AUTHOR]
- Subjects :
- *ALKENES
*PALLADIUM
*NICKEL
Subjects
Details
- Language :
- English
- ISSN :
- 00397911
- Volume :
- 50
- Issue :
- 15
- Database :
- Academic Search Index
- Journal :
- Synthetic Communications
- Publication Type :
- Academic Journal
- Accession number :
- 144690781
- Full Text :
- https://doi.org/10.1080/00397911.2020.1774903