Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Kazuhide Matsumura"'
Publikováno v:
Journal of Computer Chemistry, Japan. 11:125-130
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95cec49c26c0c806d078842cc7ba6c93
https://doi.org/10.2477/jccj.h2032
https://doi.org/10.2477/jccj.h2032
Publikováno v:
Tetrahedron Letters. 48:5807-5810
A partially benzylated derivative of the anhydro- d -altro-heptulose found in Coriaria japonica A, which is a synthetically useful unit, was successfully synthesized from a d -mannose derivative by a novel synthetic approach involving an intramolecul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4979c6d4b11771db50757e77b9bc45e6
https://doi.org/10.1016/j.tetlet.2007.06.057
https://doi.org/10.1016/j.tetlet.2007.06.057
Autor:
Toshiyuki Inazu, Takashi Yamanoi, Mikio Watanabe, Ippo Yamazaki, Yoshiki Oda, Kazuhide Matsumura, Kaname Katsuraya, Sho Matsuda
Publikováno v:
Tetrahedron. 62:10383-10392
We prepared several kinds of 1- C -alkyl-2,3,4,6-tetra- O -benzyl-α- d -glucopyranose derivatives containing methyl, ethyl, n -butyl, and benzyl groups as the alkyl groups at their anomeric positions. The Lewis acid- or Bronsted acid-catalyzed O-gly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::851bf172e9ffccdf853d4fe7b4d12a3f
https://doi.org/10.1016/j.tet.2006.08.059
https://doi.org/10.1016/j.tet.2006.08.059
Publikováno v:
Synlett. 2005:2973-2977
The intramolecular glycosidation of the 1-C-alkyl-D-hexopyranose derivatives to form the anhydroketopyranoses having 6,8-dioxabicyclo[3.2.1]octane structures was investigated. We synthesized several l-C-alkyl-2,3,4-tri-O-benzyl-D-hexopyranoses and fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5a2fbb232d015c751148b90960bcafc
https://doi.org/10.1055/s-2005-921912
https://doi.org/10.1055/s-2005-921912
Publikováno v:
ChemInform. 42
The compounds (III) and (VIII) are quantitatively converted to the corresponding compounds (IV) and (IX) by using NaOMe in MeOH.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14f1d5a97f8d21e80f2d356ac66ccec8
https://doi.org/10.1002/chin.201119186
https://doi.org/10.1002/chin.201119186
Publikováno v:
ChemInform. 37
The intramolecular glycosidation of the 1-C-alkyl-D-hexopyranose derivatives to form the anhydroketopyranoses having 6,8-dioxabicyclo[3.2.1]octane structures was investigated. We synthesized several l-C-alkyl-2,3,4-tri-O-benzyl-D-hexopyranoses and fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de5f2df875c44282bfa227656b4ebc46
https://doi.org/10.1002/chin.200616189
https://doi.org/10.1002/chin.200616189
Publikováno v:
HETEROCYCLES. 82:531
We investigated a synthetic approach to the anhydroketopyranoses having a 6,8-dioxabicyclo[3.2.1]octane structure from D -glucopyranose derivatives. The paper describes the nucleophilic addition of the organometallic reagents RLi or RMgX to the gluco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3baf08041c769a5a946d99e8aa888840
https://doi.org/10.3987/com-10-s(e)24
https://doi.org/10.3987/com-10-s(e)24