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Intramolecular N-coordination in ketiminoboranes.
- Source :
- Dalton Transactions: An International Journal of Inorganic Chemistry; 3/28/2015, Vol. 44 Issue 12, p5284-5287, 4p
- Publication Year :
- 2015
-
Abstract
- Treatment of the imine PhC(=NSiMe<subscript>3</subscript>)py with Et<subscript>2</subscript>BOMe or BF<subscript>3</subscript>·Et<subscript>2</subscript>O afforded bicyclic ketiminoboranes 4a and 4bvia intramolecular N-coordination. The basicity of the imine N is evidenced by their reactivity towards Brønsted and Lewis acids and the structures of 4a·HCl and 4b·BF<subscript>3</subscript> are reported as well as the dipyridyl imine derivative 4c·HCl. [ABSTRACT FROM AUTHOR]
- Subjects :
- IMINES
LEWIS acids
BORANES
CHEMICAL derivatives
BIPYRIDINE
Subjects
Details
- Language :
- English
- ISSN :
- 14779226
- Volume :
- 44
- Issue :
- 12
- Database :
- Complementary Index
- Journal :
- Dalton Transactions: An International Journal of Inorganic Chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 101531809
- Full Text :
- https://doi.org/10.1039/c5dt00196j