| Tartalom: |
http://real.mtak.hu/41746/ |
| Archívum: |
MTA Könyvtár |
| Gyűjtemény: |
Status = In Press
Type = Book Section
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| Cím: |
ASYMMETRIC REDUCTION OF KETONES TO CHIRAL PLATFORM MOLECULES
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| Létrehozó: |
Fridrich, Bálint
Tukacs, JĂłzsef M.
Mika, László Tamás
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| Közreműködő: |
Pályi, Gyula
Kurdi, RĂłbert
Zucci, Claudia
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| Kiadó: |
Elsevier
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| Dátum: |
2016
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| Téma: |
QD04 Organic chemistry / szerves kémia
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| Tartalmi leírás: |
The enantioselective reduction of prochiral substrates including C=O double bonds is fundamentally important in the synthesis of biologically active compounds. Due to the depletion of fossil-based resources, the production of these species from renewable resources is highly desired. The enantiopure Îł-valerolactone was proposed as a biomass-based chiral platform molecule that can be easily obtained by the asymmetric reduction of levulinic acid and its esters. Synthetic schemes of the production of optically active Îł-valerolactone are presented. The effect of catalyst composition and reaction parameters on the activity and selectivity will be discussed in detail.
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| Nyelv: |
angol
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| Típus: |
Book Section
PeerReviewed
info:eu-repo/semantics/bookPart
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| Formátum: |
text
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| Azonosító: |
Fridrich, Bálint and Tukacs, József M. and Mika, László Tamás (2016) ASYMMETRIC REDUCTION OF KETONES TO CHIRAL PLATFORM MOLECULES. In: ADVANCES IN ASYMMETRIC AUTOCATALYSIS AND RELATED TOPIC. Elsevier. (In Press)
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