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Solvent-controlled regioselective protection of allyl-4,6-benzylidene glucopyranosides
We wish to report a simple synthetic procedure, which permits the regiospecific mono-acylation, alkylation and silylation at the 2-position of allyl 4,6-O-benzylidene α-D-glucopyranoside in high yields and which does not require the use of catalysts.
| Autores principales: | , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Beilstein-Institut
2007
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2048501/ https://www.ncbi.nlm.nih.gov/pubmed/17897436 http://dx.doi.org/10.1186/1860-5397-3-26 |