Iida et al., 1987 - Google Patents
Total synthesis of (+)-nojirimycin and (+)-1-deoxynojirimycinIida et al., 1987
- Document ID
- 1258433273279249357
- Author
- Iida H
- Yamazaki N
- Kibayashi C
- Publication year
- Publication venue
- The Journal of Organic Chemistry
External Links
Snippet
2 (2) initially obtained by chemical transformation of no-jirimycin2 and L-sorvofuranose20 was first isolated from plants of genus Morus (Mori cortex) 4 as an alkaloidal component named moranoline and later also from strains of Bacillus3 and a mulberry tree (Morus …
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Classifications
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- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
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