Details
Originalsprache | Englisch |
---|---|
Seiten (von - bis) | 2905-2907 |
Seitenumfang | 3 |
Fachzeitschrift | Tetrahedron letters |
Jahrgang | 48 |
Ausgabenummer | 16 |
Publikationsstatus | Veröffentlicht - 16 Apr. 2007 |
Abstract
The synthesis of the C23-C32 fragment of spirangien A is reported using Evans' alkylation, Evans-Metternich aldol reaction and a substrate controlled stereoselective reduction.
ASJC Scopus Sachgebiete
- Biochemie, Genetik und Molekularbiologie (insg.)
- Biochemie
- Pharmakologie, Toxikologie und Pharmazie (insg.)
- Wirkstoffforschung
- Chemie (insg.)
- Organische Chemie
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in: Tetrahedron letters, Jahrgang 48, Nr. 16, 16.04.2007, S. 2905-2907.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Synthesis of the C23-C32 fragment of spirangien
AU - Lorenz, Michael
AU - Kalesse, Markus
PY - 2007/4/16
Y1 - 2007/4/16
N2 - The synthesis of the C23-C32 fragment of spirangien A is reported using Evans' alkylation, Evans-Metternich aldol reaction and a substrate controlled stereoselective reduction.
AB - The synthesis of the C23-C32 fragment of spirangien A is reported using Evans' alkylation, Evans-Metternich aldol reaction and a substrate controlled stereoselective reduction.
KW - Evans alkylation
KW - Evans-Metternich aldol
KW - Substrate controlled stereoselective reduction
UR - http://www.scopus.com/inward/record.url?scp=33947243353&partnerID=8YFLogxK
U2 - 10.1016/j.tetlet.2007.02.081
DO - 10.1016/j.tetlet.2007.02.081
M3 - Article
AN - SCOPUS:33947243353
VL - 48
SP - 2905
EP - 2907
JO - Tetrahedron letters
JF - Tetrahedron letters
SN - 0040-4039
IS - 16
ER -