Details
| Originalsprache | Englisch |
|---|---|
| Seiten (von - bis) | 837-838 |
| Seitenumfang | 2 |
| Fachzeitschrift | SYNLETT |
| Jahrgang | 1995 |
| Ausgabenummer | 8 |
| Publikationsstatus | Veröffentlicht - Aug. 1995 |
Abstract
The reduction of chiral β-keto esters with baker's yeast is described. Reduction of 10 yields highly functionalized diol 11 with excellent stereoselectivity and generates a useful intermediate for natural product syntheses.
ASJC Scopus Sachgebiete
- Chemie (insg.)
- Organische Chemie
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in: SYNLETT, Jahrgang 1995, Nr. 8, 08.1995, S. 837-838.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Remarkable kinetic resolution of chiral β-keto esters by baker's yeast reduction
AU - Eh, Marcus
AU - Kalesse, Markus
N1 - Publisher Copyright: © 1995 Georg Thieme Verlag, Rudigerstr. 14, 70469 Stuttgart, Germany. All rights reserved.
PY - 1995/8
Y1 - 1995/8
N2 - The reduction of chiral β-keto esters with baker's yeast is described. Reduction of 10 yields highly functionalized diol 11 with excellent stereoselectivity and generates a useful intermediate for natural product syntheses.
AB - The reduction of chiral β-keto esters with baker's yeast is described. Reduction of 10 yields highly functionalized diol 11 with excellent stereoselectivity and generates a useful intermediate for natural product syntheses.
KW - 1,3-diols
KW - Baker's yeast reduction
KW - kinetic resolution
KW - β-keto esters
UR - http://www.scopus.com/inward/record.url?scp=0013350761&partnerID=8YFLogxK
U2 - 10.1055/s-1995-5083
DO - 10.1055/s-1995-5083
M3 - Article
AN - SCOPUS:0013350761
VL - 1995
SP - 837
EP - 838
JO - SYNLETT
JF - SYNLETT
SN - 0936-5214
IS - 8
ER -