Details
| Translated title of the contribution | Cyclopentanole durch eine Silicium-induzierte Reaktionskaskade |
|---|---|
| Original language | English |
| Pages (from-to) | 217-218 |
| Number of pages | 2 |
| Journal | Angewandte Chemie International Edition in English |
| Volume | 33 |
| Issue number | 2 |
| Publication status | Published - 1 Feb 1994 |
| Externally published | Yes |
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 subject areas
- Chemical Engineering(all)
- Catalysis
- Chemistry(all)
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In: Angewandte Chemie International Edition in English, Vol. 33, No. 2, 01.02.1994, p. 217-218.
Research output: Contribution to journal › Article › Research › 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 -