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Simple Metal-Free Direct Reductive Amination Using Hydrosilatrane to Form Secondary and Tertiary Amines.
- Source :
-
Advanced Synthesis & Catalysis . 6/6/2017, Vol. 359 Issue 11, p1872-1878. 7p. - Publication Year :
- 2017
-
Abstract
- This work describes the use of cheap, safe, and easy-to-handle hydrosilatrane as the reductant in direct reductive amination reactions. This efficient method enables a facile, metal-free access to secondary and tertiary amines from a wide range of aldehydes and ketones, with the synthesis of tertiary amines requiring no additives at all. This reaction demonstrates excellent functional group tolerance, chemoselectivity, and scalability. [ABSTRACT FROM AUTHOR]
- Subjects :
- *AMINATION
*TERTIARY amines
*CHEMICAL reactions
*ALDEHYDES
*KETONES
*CHEMOSELECTIVITY
Subjects
Details
- Language :
- English
- ISSN :
- 16154150
- Volume :
- 359
- Issue :
- 11
- Database :
- Academic Search Index
- Journal :
- Advanced Synthesis & Catalysis
- Publication Type :
- Academic Journal
- Accession number :
- 123439519
- Full Text :
- https://doi.org/10.1002/adsc.201700079