Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Sho Matsuda"'
Publikováno v:
Sports Medicine - Open, Vol 3, Iss 1, Pp 1-7 (2017)
Abstract Background There is a large amount of information regarding risk factors for fifth metatarsal stress fractures; however, there are few studies involving large numbers of subjects. This study aimed to compare the static foot alignment and dis
Externí odkaz:
https://doaj.org/article/bd6beba35f4d48bab349185bb172b923
Publikováno v:
Molecules, Vol 13, Iss 8, Pp 1840-1845 (2008)
Abstract: This paper describes a synthetic approach to a novel D-glucose-conjugated 15-crown-5 ether having a spiroketal structure starting from a 1-C-vinylated glucose derivative. The approach consists of the glycosylation of the vinylated glucose d
Externí odkaz:
https://doaj.org/article/3d7d75cf06194a5785be990ab69686eb
Publikováno v:
Sports Medicine-Open, Vol 3, Iss 1, Pp 1-7 (2017)
Sports Medicine-Open
Sports Medicine-Open
Background There is a large amount of information regarding risk factors for fifth metatarsal stress fractures; however, there are few studies involving large numbers of subjects. This study aimed to compare the static foot alignment and distribution
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf129cf6ec31148ffe8aed41b151e862
https://doi.org/10.1186/s40798-017-0095-y
https://doi.org/10.1186/s40798-017-0095-y
Publikováno v:
Tetrahedron Letters. 55:6394-6398
This Letter describes a stereoselective synthetic approach to spiro[5.5]ketals from the exo-glucals, constructed from 1-(4-hydroxyalkylidene)-1,5-anhydro- d -glucitol, by spirocyclization based on intramolecular α- and β-selective glycosylation. St
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2a26e87e393184395ea1cb9a2ed2a3d
https://doi.org/10.1016/j.tetlet.2014.09.095
https://doi.org/10.1016/j.tetlet.2014.09.095
Publikováno v:
Supramolecular Chemistry. 21:638-642
This study describes the 2D 1H and 13C diffusion-ordered NMR spectroscopy (DOSY) experiments using the mixed sample of α-cyclodextrin (α-CyD) and phenyl β-d-(13C6)glucopyranoside (1). Both the 2D 1H and 13C DOSY spectra showed the component with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::daa28bf686547305d997c01313e10453
https://doi.org/10.1080/10610270802709345
https://doi.org/10.1080/10610270802709345
Publikováno v:
Tetrahedron. 64:8082-8088
A partially benzylated derivative of 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 the intramolecular
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddb9a849ad6b6ccbfdaa3349cc6f165d
https://doi.org/10.1016/j.tet.2008.06.068
https://doi.org/10.1016/j.tet.2008.06.068
Publikováno v:
Molecules
Molecules, Vol 13, Iss 8, Pp 1840-1845 (2008)
Volume 13
Issue 8
Pages 1840-1845
Molecules, Vol 13, Iss 8, Pp 1840-1845 (2008)
Volume 13
Issue 8
Pages 1840-1845
This paper describes a synthetic approach to a novel D-glucose-conjugated 15-crown-5 ether having a spiroketal structure starting from a 1-C-vinylated glucose derivative. The approach consists of the glycosylation of the vinylated glucose derivative
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::871e1162fb36423a6ffdc52955092583
http://europepmc.org/articles/PMC6245333
http://europepmc.org/articles/PMC6245333
Publikováno v:
Carbohydrate Research. 343:1366-1372
Several partially benzylated mono-, di-, and trisaccharides having an anomeric hydroxyl group were successfully prepared by selective cleavage of the β-fructofuranosidic linkage in fully benzylated sucrose and sucrose-related oligosaccharides derive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f593aab8e261cb0e7f31fd7733b82f4
https://doi.org/10.1016/j.carres.2008.03.024
https://doi.org/10.1016/j.carres.2008.03.024
Publikováno v:
Letters in Organic Chemistry. 5:30-33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a40c87293ea457e99bd7dc7cfe9d1d0f
https://doi.org/10.2174/157017808783330289
https://doi.org/10.2174/157017808783330289
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