Abstract
A novel, one-step synthesis of substituted pyridine- and quinoline-derivatives was achieved by acceptorless dehydrogenative coupling of γ-aminoalcohols with secondary alcohols. The reaction involves consecutive C-N and C-C bond formation, catalyzed by a bipyridyl-based ruthenium pincer complex with a base.
| Original language | English |
|---|---|
| Pages (from-to) | 6632-6634 |
| Number of pages | 3 |
| Journal | Chemical Communications |
| Volume | 49 |
| Issue number | 59 |
| DOIs | |
| Publication status | Published - Jul 28 2013 |
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ASJC Scopus subject areas
- Metals and Alloys
- Materials Chemistry
- Surfaces, Coatings and Films
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- Catalysis
- Chemistry(all)
Cite this
Direct synthesis of pyridines and quinolines by coupling of γ-amino-alcohols with secondary alcohols liberating H2 catalyzed by ruthenium pincer complexes. / Srimani, Dipankar; Ben-David, Yehoshoa; Milstein, David.
In: Chemical Communications, Vol. 49, No. 59, 28.07.2013, p. 6632-6634.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Direct synthesis of pyridines and quinolines by coupling of γ-amino-alcohols with secondary alcohols liberating H2 catalyzed by ruthenium pincer complexes
AU - Srimani, Dipankar
AU - Ben-David, Yehoshoa
AU - Milstein, David
PY - 2013/7/28
Y1 - 2013/7/28
N2 - A novel, one-step synthesis of substituted pyridine- and quinoline-derivatives was achieved by acceptorless dehydrogenative coupling of γ-aminoalcohols with secondary alcohols. The reaction involves consecutive C-N and C-C bond formation, catalyzed by a bipyridyl-based ruthenium pincer complex with a base.
AB - A novel, one-step synthesis of substituted pyridine- and quinoline-derivatives was achieved by acceptorless dehydrogenative coupling of γ-aminoalcohols with secondary alcohols. The reaction involves consecutive C-N and C-C bond formation, catalyzed by a bipyridyl-based ruthenium pincer complex with a base.
UR - http://www.scopus.com/inward/record.url?scp=84879765990&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84879765990&partnerID=8YFLogxK
U2 - 10.1039/c3cc43227k
DO - 10.1039/c3cc43227k
M3 - Article
C2 - 23771175
AN - SCOPUS:84879765990
VL - 49
SP - 6632
EP - 6634
JO - Chemical Communications
JF - Chemical Communications
SN - 1359-7345
IS - 59
ER -