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 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
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Hosokawa, S., Kirschbaum, B., & Isobe, M. (1998). 1,4-anti induction in C-glycosylation of pentose glycals. Tetrahedron Letters, 39(14), 1917-1920. https://doi.org/10.1016/S0040-4039(98)00047-1