| Autor: |
Phanumartwiwath A; School of Chemistry, University of Bristol , Cantock's Close, Bristol BS8 1TS, U.K., Hornsby TW, Jamalis J, Bailey CD, Willis CL |
| Jazyk: |
angličtina |
| Zdroj: |
Organic letters [Org Lett] 2013 Nov 15; Vol. 15 (22), pp. 5734-7. Date of Electronic Publication: 2013 Oct 28. |
| DOI: |
10.1021/ol402760p |
| Abstrakt: |
A versatile method for the synthesis of orthogonally protected D-xylose 1-thioethers is described using unusual silyl group migrations which were pivotal in the synthesis of 4,8-dimethyl-6-O-(2',4'-di-O-methyl-β-D-xylopyranosyl)hydroxyquinoline confirming the structure and absolute configuration of the natural product. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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