Details
| Original language | English |
|---|---|
| Pages (from-to) | 289-290 |
| Number of pages | 2 |
| Journal | Synlett |
| Volume | 1993 |
| Issue number | 4 |
| Publication status | Published - Apr 1993 |
| Externally published | Yes |
Abstract
The direct regioselective synthesis of hex-1-enopyran-3-uloses 3, 6, 8, and 10 by oxidation of the corresponding per-O-acylated and per-O-benzylated glycals 1, 4, 5, 7, and 9 is described. The method involves the use of [hydroxy(tosyloxy)-iodo]benzene 2.
ASJC Scopus subject areas
- Chemistry(all)
- Organic Chemistry
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In: Synlett, Vol. 1993, No. 4, 04.1993, p. 289-290.
Research output: Contribution to journal › Article › Research › peer review
}
TY - JOUR
T1 - Regioselective Oxidation of Glycals with Hypervalent Iodine Reagents
AU - Kirschning, Andreas
AU - Dräger, Gerald
AU - Harders, Jan
PY - 1993/4
Y1 - 1993/4
N2 - The direct regioselective synthesis of hex-1-enopyran-3-uloses 3, 6, 8, and 10 by oxidation of the corresponding per-O-acylated and per-O-benzylated glycals 1, 4, 5, 7, and 9 is described. The method involves the use of [hydroxy(tosyloxy)-iodo]benzene 2.
AB - The direct regioselective synthesis of hex-1-enopyran-3-uloses 3, 6, 8, and 10 by oxidation of the corresponding per-O-acylated and per-O-benzylated glycals 1, 4, 5, 7, and 9 is described. The method involves the use of [hydroxy(tosyloxy)-iodo]benzene 2.
UR - http://www.scopus.com/inward/record.url?scp=84988065051&partnerID=8YFLogxK
U2 - 10.1055/s-1993-22435
DO - 10.1055/s-1993-22435
M3 - Article
AN - SCOPUS:84988065051
VL - 1993
SP - 289
EP - 290
JO - Synlett
JF - Synlett
SN - 0936-5214
IS - 4
ER -