Preparation of 1,2,3,4,6-penta-O-galloyl-[U-14C]-D-glucopyranose
✍ Scribed by Yumin Chen; Ann E. Hagerman; Robert E. Minto
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- French
- Weight
- 105 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0022-2135
- DOI
- 10.1002/jlcr.648
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✦ Synopsis
Abstract
The synthesis of 1,2,3,4,6‐penta‐O‐galloyl‐[U‐^14^C]‐D‐glucopyranose is described. [U‐^14^C] glucopyranose was reacted with tri‐O‐benzylgallic acid forming 1,2,3,4,6‐penta(tri‐O‐benzylgalloyl)‐[U‐^14^C]‐D‐glucopyranose as chromatograpically separable anomers. Removal of the benzyl group by catalytic hydrogenation afforded 1,2,3,4,6‐penta‐O‐galloyl‐[U‐^14^C]‐D‐glucopyranose in 54% overall yield. Copyright © 2002 John Wiley & Sons, Ltd.
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