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| Titel in Übersetzung | Cyclopentanole durch eine Silicium-induzierte Reaktionskaskade |
|---|---|
| Originalsprache | Englisch |
| Seiten (von - bis) | 217-218 |
| Seitenumfang | 2 |
| Fachzeitschrift | Angewandte Chemie International Edition in English |
| Jahrgang | 33 |
| Ausgabenummer | 2 |
| Publikationsstatus | Veröffentlicht - 1 Feb. 1994 |
| Extern publiziert | Ja |
Abstract
Through the rare [4 + 1] construction strategy, the cyclopentanols 1 are accessible by a sequence of epoxide ring opening, silyl migration, and tosylate substitution. Optically active and annelated cyclopentanols can also be prepared by this route. (Figure Presented.)
ASJC Scopus Sachgebiete
- Chemische Verfahrenstechnik (insg.)
- Katalyse
- Chemie (insg.)
- Allgemeine Chemie
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in: Angewandte Chemie International Edition in English, Jahrgang 33, Nr. 2, 01.02.1994, S. 217-218.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - Syntheses of Cyclopentanols by a Silicon‐Induced Cascade Reaction
AU - Fischer, Michael‐Ralph ‐R
AU - Kirschning, Andreas
AU - Michel, Tycho
AU - Schaumann, Ernst
PY - 1994/2/1
Y1 - 1994/2/1
N2 - Through the rare [4 + 1] construction strategy, the cyclopentanols 1 are accessible by a sequence of epoxide ring opening, silyl migration, and tosylate substitution. Optically active and annelated cyclopentanols can also be prepared by this route. (Figure Presented.)
AB - Through the rare [4 + 1] construction strategy, the cyclopentanols 1 are accessible by a sequence of epoxide ring opening, silyl migration, and tosylate substitution. Optically active and annelated cyclopentanols can also be prepared by this route. (Figure Presented.)
UR - http://www.scopus.com/inward/record.url?scp=33748220606&partnerID=8YFLogxK
U2 - 10.1002/anie.199402171
DO - 10.1002/anie.199402171
M3 - Article
AN - SCOPUS:33748220606
VL - 33
SP - 217
EP - 218
JO - Angewandte Chemie International Edition in English
JF - Angewandte Chemie International Edition in English
SN - 0570-0833
IS - 2
ER -