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Preparation and structural determination of methyl 3-C-p-tolylsulfonyl-2-C-p-tolylthio-β-d-glucopyanoside derivatives and their 5a-carba-dl-analogs having non-chair conformation in solutions

✍ Scribed by Tohru Sakakibara; Kiyotaka Suzuki; Akiko Sakai; Miwa Shindo; Chihiro Nagano; Shinya Narumi; Yasuhiro Kajihara; Katsura Mochizuki


Publisher
Elsevier Science
Year
2003
Tongue
French
Weight
248 KB
Volume
44
Category
Article
ISSN
0040-4039

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✦ Synopsis


Methyl 4,6-O-benzylidene-2,3-dideoxy-3-C-p-tolylsulfonyl-2-C-p-tolylthio-b-D-glucopyranoside and its 5a-carba-DLanalog exit mainly in a non-chair conformation in solutions, but the latter occupies a chair conformation in a solid state.


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X-ray crystal structures of 1,2,4-tri-O-
✍ Thomas Richter; Peter Luger; Tadashi Hanaya; Hiroshi Yamamoto 📂 Article 📅 1991 🏛 Elsevier Science 🌐 English ⚖ 780 KB

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