Výsledky vyhledávání - "Takako Tashiro"

Synthesis of MethylO-α-D-Mannosyl-(1→4)-[(3-O-methyl-α-D- mannosyl)-(1→4)-]n3-O-methyl-α-D-mannosides (n= 0, 1, and 2) via Dehydrative Glycosylation

Autor: Shinkiti Koto, Ayano Takabatake, Megumi Terayama, Asako Miura, Motoko Hirooka, Emi Mitani, Takako Tashiro, Kayo Chiba

Publikováno v: Bulletin of the Chemical Society of Japan. 75:1301-1309

Methyl O-α-D-mannopyranosyl-(1→4)-[(3-O-methyl-α-D-mannopyranosyl-(1→4)-]n3-O-methyl-α-D-mannopyranosides (n = 0, 1, and 2), the lowest homologs related to the 3-O-methylmannose polysaccharides (MMP) from Mycobacterium smegmatis, were synthesi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f047dab2e680975d16a2fd013205c1e9
https://doi.org/10.1246/bcsj.75.1301

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ChemInform Abstract: Synthesis of Methyl O-α-D-Mannosyl-(1→4)- [(3-O-methyl-α-D-mannosyl)-(1→4)-] n3-O-methyl-α-D-mannosides (n = 0, 1, and 2) via Dehydrative Glycosylation

Autor: Ayano Takabatake, Shinkiti Koto, Emi Mitani, Motoko Hirooka, Kayo Chiba, Asako Miura, Megumi Terayama, Takako Tashiro

Publikováno v: ChemInform. 33

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b9cdc8f599e9b72759ac8f34aa5910e2
https://doi.org/10.1002/chin.200236203

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Hydrophobic Vitamin B12. V. Electrochemical Carbon-Skeleton Rearrangement as Catalyzed by Hydrophobic Vitamin B12: Reaction Mechanisms and Migratory Aptitude of Functional Groups

Autor: Yoshio Hisaeda, Teruhisa Ohno, Yutaro Tani, Takako Tashiro, Yoshihisa Matsuda, Yukito Murakami, Toshiaki Ozaki

Publikováno v: Bulletin of the Chemical Society of Japan. 60:311-324

The carbon-skeleton rearrangements as catalyzed by heptamethyl cobyrinate perchlorate, [Cob(II)7C1ester]ClO4, were investigated under electrochemical conditions. The controlled-potential electrolysis of 2,2-bis(ethoxycarbonyl)-1-bromopropane, which i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::bdcab49788a9b29e45d06490bdb046c5
https://doi.org/10.1246/bcsj.60.311

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REACTION MECHANISMS FOR ELECTROCHEMICAL CARBON-SKELETON REARRANGEMENT AS CATALYZED BY HYDROPHOBIC VITAMIN B12IN NONAQUEOUS MEDIA

Autor: Yukito Murakami, Yoshio Hisaeda, Yoshihisa Matsuda, Takako Tashiro

Publikováno v: Chemistry Letters. 15:555-558

Reaction mechanisms for the controlled-potential electrolysis of 2,2-bis(ethoxycarbonyl)-1-bromopropane at −1.0, −1.5, and −2.0 V vs. SCE as catalyzed by a hydrophobic vitamin B12 were clarified. The carbon-skeleton rearrangement was postulated

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::141b51a28cf4e48afe342290c818d5a7
https://doi.org/10.1246/cl.1986.555

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ELECTROCHEMICAL CARBON-SKELETON REARRANGEMENT AS CATALYZED BY HYDROPHOBIC VITAMIN B12IN NONAQUEOUS MEDIA

Autor: Yukito Murakami, Yoshio Hisaeda, Yoshihisa Matsuda, Takako Tashiro

Publikováno v: Chemistry Letters. 14:1813-1816

The controlled-potential electrolysis of 2,2-bis(ethoxycarbonyl)-1-bromopropane at −1.50 V vs. SCE as catalyzed by a hydrophobic vitamin B12 in DMF proceeded to give 1,2-bis(ethoxycarbonyl)propane as a major product in the presence of acetic acid u

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c7c8cd7a25d8150acc0e4763aeb7d5c5
https://doi.org/10.1246/cl.1985.1813

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