Abstract
The reaction of pantolactone derived bicyclic acetal 1 with alkyl lithiums provides 2,2,4-trisubstituted 3-hydroxy oxetane 2 with high diastereoselectivity.
| Original language | English |
|---|---|
| Pages (from-to) | 651-654 |
| Number of pages | 4 |
| Journal | Synlett |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - Mar 9 2004 |
| Externally published | Yes |
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All Science Journal Classification (ASJC) codes
- Organic Chemistry
Cite this
Anionic ring-contraction reaction of cyclic acetal system : Stereoselective approach to multi-functionalized oxetanes. / Suzuki, Masaki; Tomooka, Katsuhiko.
In: Synlett, No. 4, 09.03.2004, p. 651-654.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Anionic ring-contraction reaction of cyclic acetal system
T2 - Stereoselective approach to multi-functionalized oxetanes
AU - Suzuki, Masaki
AU - Tomooka, Katsuhiko
PY - 2004/3/9
Y1 - 2004/3/9
N2 - The reaction of pantolactone derived bicyclic acetal 1 with alkyl lithiums provides 2,2,4-trisubstituted 3-hydroxy oxetane 2 with high diastereoselectivity.
AB - The reaction of pantolactone derived bicyclic acetal 1 with alkyl lithiums provides 2,2,4-trisubstituted 3-hydroxy oxetane 2 with high diastereoselectivity.
UR - http://www.scopus.com/inward/record.url?scp=1642293099&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=1642293099&partnerID=8YFLogxK
U2 - 10.1055/s-2004-817772
DO - 10.1055/s-2004-817772
M3 - Article
AN - SCOPUS:1642293099
SP - 651
EP - 654
JO - Synlett
JF - Synlett
SN - 0936-5214
IS - 4
ER -