Details
Original language | English |
---|---|
Pages (from-to) | 363-366 |
Number of pages | 4 |
Journal | Tetrahedron Asymmetry |
Volume | 14 |
Issue number | 3 |
Publication status | Published - 31 Jan 2003 |
Abstract
Condensation of pyruvate and acrolein with whole cells of baker's yeast resulted in a mixture of 3-hydroxy-1-penten-4-one 1 and 4-hydroxy-1-penten-3-one 2. The absolute configuration (R) and the enantiomeric excess (ee 72%) of the compound 1 were determined.
ASJC Scopus subject areas
- Chemical Engineering(all)
- Catalysis
- Chemistry(all)
- Physical and Theoretical Chemistry
- Chemistry(all)
- Organic Chemistry
- Chemistry(all)
- Inorganic Chemistry
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In: Tetrahedron Asymmetry, Vol. 14, No. 3, 31.01.2003, p. 363-366.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Enantiogenic synthesis of (R)-(-)-3-hydroxy-1-penten-4-one
AU - Kurniadi, Toshinari H.
AU - Bel Rhlid, Rachid
AU - Juillerat, Marcel A.
AU - Schüler, Martin
AU - Berger, Ralf G.
PY - 2003/1/31
Y1 - 2003/1/31
N2 - Condensation of pyruvate and acrolein with whole cells of baker's yeast resulted in a mixture of 3-hydroxy-1-penten-4-one 1 and 4-hydroxy-1-penten-3-one 2. The absolute configuration (R) and the enantiomeric excess (ee 72%) of the compound 1 were determined.
AB - Condensation of pyruvate and acrolein with whole cells of baker's yeast resulted in a mixture of 3-hydroxy-1-penten-4-one 1 and 4-hydroxy-1-penten-3-one 2. The absolute configuration (R) and the enantiomeric excess (ee 72%) of the compound 1 were determined.
UR - http://www.scopus.com/inward/record.url?scp=0037423120&partnerID=8YFLogxK
U2 - 10.1016/S0957-4166(02)00800-5
DO - 10.1016/S0957-4166(02)00800-5
M3 - Article
AN - SCOPUS:0037423120
VL - 14
SP - 363
EP - 366
JO - Tetrahedron Asymmetry
JF - Tetrahedron Asymmetry
SN - 0957-4166
IS - 3
ER -