Abstract
Acylation of secondary alcohols using non-activated esters, in particular symmetrical esters (such as ethyl acetate), is achieved under neutral conditions with the liberation of molecular hydrogen. This unprecedented, environmentally benign reaction is homogenously catalyzed by a dearomatized ruthenium pincer PNN complex.
| Original language | English |
|---|---|
| Pages (from-to) | 3169-3173 |
| Number of pages | 5 |
| Journal | Advanced Synthesis and Catalysis |
| Volume | 352 |
| Issue number | 18 |
| DOIs | |
| Publication status | Published - Dec 17 2010 |
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Keywords
- acylation
- dehydrogenation
- homogeneous catalysis
- ruthenium pincer complex
- transesterification
ASJC Scopus subject areas
- Catalysis
- Organic Chemistry
Cite this
Ruthenium pincer-catalyzed acylation of alcohols using esters with liberation of hydrogen under neutral conditions. / Gnanaprakasam, Boopathy; Ben-David, Yehoshoa; Milstein, David.
In: Advanced Synthesis and Catalysis, Vol. 352, No. 18, 17.12.2010, p. 3169-3173.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Ruthenium pincer-catalyzed acylation of alcohols using esters with liberation of hydrogen under neutral conditions
AU - Gnanaprakasam, Boopathy
AU - Ben-David, Yehoshoa
AU - Milstein, David
PY - 2010/12/17
Y1 - 2010/12/17
N2 - Acylation of secondary alcohols using non-activated esters, in particular symmetrical esters (such as ethyl acetate), is achieved under neutral conditions with the liberation of molecular hydrogen. This unprecedented, environmentally benign reaction is homogenously catalyzed by a dearomatized ruthenium pincer PNN complex.
AB - Acylation of secondary alcohols using non-activated esters, in particular symmetrical esters (such as ethyl acetate), is achieved under neutral conditions with the liberation of molecular hydrogen. This unprecedented, environmentally benign reaction is homogenously catalyzed by a dearomatized ruthenium pincer PNN complex.
KW - acylation
KW - dehydrogenation
KW - homogeneous catalysis
KW - ruthenium pincer complex
KW - transesterification
UR - http://www.scopus.com/inward/record.url?scp=78650345516&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=78650345516&partnerID=8YFLogxK
U2 - 10.1002/adsc.201000663
DO - 10.1002/adsc.201000663
M3 - Article
AN - SCOPUS:78650345516
VL - 352
SP - 3169
EP - 3173
JO - Journal fur Praktische Chemie
JF - Journal fur Praktische Chemie
SN - 1436-9966
IS - 18
ER -