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Influence of the O3 Protecting Group on Stereoselectivity in the Preparation of C-Mannopyranosides with 4,6-O-Benzylidene Protected Donors
[Image: see text] α-C-glucopyranosides and mannopyranosides are obtained in 65–85% yields from 4,6-O-benzylidene-protected glucosyl and mannosyl thioglycosides bearing ester functionality at the 3-O-position by coupling reaction with C-nucleophiles on activation with diphenyl sulfoxide, 2,4,6-tri-te...
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| Main Authors: | , |
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| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2010
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3064765/ https://ncbi.nlm.nih.gov/pubmed/21070063 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jo101453y |
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