Abstract
The C-glycosylation of pentose glycals with silylacetylenes or allylsilanes via oxocarbenium ion intermediates proceeded under high regio- and stereoselectivity giving the 1,4-anti products as the predominant products.
| Original language | English |
|---|---|
| Pages (from-to) | 1917-1920 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 39 |
| Issue number | 14 |
| DOIs | |
| Publication status | Published - 1998 Apr 2 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Biochemistry
- Organic Chemistry
- Drug Discovery
Cite this
1,4-anti induction in C-glycosylation of pentose glycals. / Hosokawa, Seijiro; Kirschbaum, Bettina; Isobe, Minoru.
In: Tetrahedron Letters, Vol. 39, No. 14, 02.04.1998, p. 1917-1920.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - 1,4-anti induction in C-glycosylation of pentose glycals
AU - Hosokawa, Seijiro
AU - Kirschbaum, Bettina
AU - Isobe, Minoru
PY - 1998/4/2
Y1 - 1998/4/2
N2 - The C-glycosylation of pentose glycals with silylacetylenes or allylsilanes via oxocarbenium ion intermediates proceeded under high regio- and stereoselectivity giving the 1,4-anti products as the predominant products.
AB - The C-glycosylation of pentose glycals with silylacetylenes or allylsilanes via oxocarbenium ion intermediates proceeded under high regio- and stereoselectivity giving the 1,4-anti products as the predominant products.
UR - http://www.scopus.com/inward/record.url?scp=0032473853&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0032473853&partnerID=8YFLogxK
U2 - 10.1016/S0040-4039(98)00047-1
DO - 10.1016/S0040-4039(98)00047-1
M3 - Article
AN - SCOPUS:0032473853
VL - 39
SP - 1917
EP - 1920
JO - Tetrahedron Letters
JF - Tetrahedron Letters
SN - 0040-4039
IS - 14
ER -