## Abstract Ring‐opening polymerization of a new anhydro ribose‐type monomer, 1,4‐anhydro‐3‐azido‐3‐deoxy‐2‐__O‐tert__‐butyldimethylsilyl‐α‐D‐ribopyranose (A3ASR), was investigated. The monomer was synthesized from 1,4‐anhyro‐α‐D‐xylopyranose by three steps comprising Walden inversion at the C3 pos
✦ LIBER ✦
Production of a group-specific antibody to 1α,25-dihydroxyvitamin D and its derivatives having the 1α,3β-dihydroxylated A-ring structure
✍ Scribed by Norihiro Kobayashi; Akiko Takama; Kazuko Shiomura; Yoshimi Tabata; Kanako Takagi; Kazutake Shimada
- Book ID
- 116065887
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 868 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0039-128X
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X-ray crystallographic analyses are reported for the two title compounds (8 and 9), of which the former crystallized in two modifications (8n and 8b). In all three structures, the pyranose rings have the %, (D) conformation and the substituents at C-l are axial and those at C-24-4 are equatorial. Th