Abstract
A nickel-phosphine complex was found to be effective as the catalyst for the transformation of alcohols into β-enaminones, which was successively converted into γ-amino alcohols by a conventional reductant. The sequential transformation is equivalent to the carbon-nitrogen bond formation at the γ-position of saturated alcohols.
Original language | English |
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Pages (from-to) | 1303-1307 |
Number of pages | 5 |
Journal | Synlett |
Issue number | 9 |
DOIs | |
Publication status | Published - 2011 |
All Science Journal Classification (ASJC) codes
- Organic Chemistry