Details
| Original language | English |
|---|---|
| Pages (from-to) | 2905-2907 |
| Number of pages | 3 |
| Journal | Tetrahedron letters |
| Volume | 48 |
| Issue number | 16 |
| Publication status | Published - 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.
Keywords
- Evans alkylation, Evans-Metternich aldol, Substrate controlled stereoselective reduction
ASJC Scopus subject areas
- Biochemistry, Genetics and Molecular Biology(all)
- Biochemistry
- Pharmacology, Toxicology and Pharmaceutics(all)
- Drug Discovery
- Chemistry(all)
- Organic Chemistry
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In: Tetrahedron letters, Vol. 48, No. 16, 16.04.2007, p. 2905-2907.
Research output: Contribution to journal › Article › Research › 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 -