Details
| Original language | English |
|---|---|
| Pages (from-to) | 1481-1483 |
| Number of pages | 3 |
| Journal | Journal of the Chemical Society, Perkin Transactions 1 |
| Issue number | 5 |
| Publication status | Published - 1990 |
| Externally published | Yes |
Abstract
In the presence of hypervalent iodine reagents, silyl-substituted δ,ε-unsaturated alcohols (4a-f) underwent ring-closure to give the pyran-3-ones (5) as well as tosyloxy substituted tetrahydropyrans (6) and (7).
ASJC Scopus subject areas
- Chemistry(all)
- General Chemistry
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In: Journal of the Chemical Society, Perkin Transactions 1, No. 5, 1990, p. 1481-1483.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Perkin communications
T2 - Iodonium-induced cyclisations of 5-silylalk-4-enols
AU - Schaumann, Ernst
AU - Kirschning, Andreas
PY - 1990
Y1 - 1990
N2 - In the presence of hypervalent iodine reagents, silyl-substituted δ,ε-unsaturated alcohols (4a-f) underwent ring-closure to give the pyran-3-ones (5) as well as tosyloxy substituted tetrahydropyrans (6) and (7).
AB - In the presence of hypervalent iodine reagents, silyl-substituted δ,ε-unsaturated alcohols (4a-f) underwent ring-closure to give the pyran-3-ones (5) as well as tosyloxy substituted tetrahydropyrans (6) and (7).
UR - http://www.scopus.com/inward/record.url?scp=37049081769&partnerID=8YFLogxK
U2 - 10.1039/P19900001481
DO - 10.1039/P19900001481
M3 - Article
AN - SCOPUS:37049081769
SP - 1481
EP - 1483
JO - Journal of the Chemical Society, Perkin Transactions 1
JF - Journal of the Chemical Society, Perkin Transactions 1
SN - 1470-4358
IS - 5
ER -