p-Nitrophenyl alpha-maltopentaoside, having a benzyl group on O-6 of the terminal (nonreducing) D-glucosyl group was prepared by use of a reductive ring-opening reaction. Highly regioselective reduction of p-nitrophenyl O-(2,3-di-O-benzoyl-4,6-O-benzylidene-alpha-D-glucopyranosyl)-(1----4)- tris[O-(
✦ LIBER ✦
Preparation of carboxymethyl derivatives of p-nitrophenyl α-maltopentaoside as substrate of α-amylases
✍ Scribed by Shinji Satomura; Kaoru Omichi; Tokuji Ikenaka
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 537 KB
- Volume
- 180
- Category
- Article
- ISSN
- 0008-6215
No coin nor oath required. For personal study only.
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