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• W2146195175 abstract "A new class of molecules with a triptycene rigid core surrounded by six monosaccharide residues was synthesized. Hexakis(bromomethyl) substituted triptycene was converted into a six-armed triptycene azide (2,3,6,7,14,15-hexakis(azidomethyl)-9,10-dihydro-9,10-[1’,2’]benzenoanthracene). The key step of the synthesis was the cycloaddition of the azide to 2-propyn-1-yl β-D-gluco- or galactopyranosides. All products were isolated in good yields and were fully characterized." @default.
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• W2146195175 date "2013-11-08" @default.
• W2146195175 modified "2023-10-18" @default.
• W2146195175 title "Synthesis of enantiopure sugar-decorated six-armed triptycene derivatives" @default.
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• W2146195175 doi "https://doi.org/10.3762/bjoc.9.278" @default.
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