Sato et al., 1994 - Google Patents
Total Synthesis of a Novel,. BETA.-Glucosidase Inhibitor, Cyclophellitol Starting from D-Glucose.Sato et al., 1994
View PDF- Document ID
- 14083696090629180819
- Author
- Sato K
- Bokura M
- Moriyama H
- Igarashi T
- Publication year
- Publication venue
- Chemistry letters
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Snippet
Rokkakubashi, Kanagawa-ku, Yokohama 221 Page 1 CHEMISTRY LETTERS, pp. 37-40,
1994. © 1994 The Chemical Society of Japan Total Synthesis of a Novel ß-Glucosidase
Inhibitor, Cyclophellitol Starting from D-Glucose Ken-ichi SATO,* Masayuki BOKURA …
- YQLWKYQDOQEWRD-GEGSFZHJSA-N (1R,2R,3R,4S,5R,6S)-2-(hydroxymethyl)-7-oxabicyclo[4.1.0]heptane-3,4,5-triol data:image/svg+xml;base64,<?xml version='1.0' encoding='iso-8859-1'?>
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 O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)[C@H]2O[C@H]21 0 title abstract description 8
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
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