Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Hiroko Kakuda"'
Publikováno v:
Bulletin of the Chemical Society of Japan. 86:620-627
Activation of dioxygen in the heme system is observed in an artificial aqueous model system. It has been demonstrated that in the system of a water-soluble hemin, tetrakis(N-methylpyridyl)porphinat...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd178475b5f13eb77d9702b3f0d9e200
https://doi.org/10.1246/bcsj.20120328
https://doi.org/10.1246/bcsj.20120328
Autor:
Koichi Inoue, Hiroko Kakuda, Hajime Yokoyama, Ken‐ichiro Awasaguchi, Masahiro Miyazawa, Ikuyo Uoya, Yoshiro Hirai, Koji Nakamura
Publikováno v:
Synlett. 2010:2392-2396
Spiro C-arylglycoriboside was synthesized in 21 steps via Pd(II)-catalyzed spirocyclization as a key reaction. Hemiketal was obtained in 47% overall yield from cis-2-butene-1,4-diol and spirocyclized with PdCl 2 (PhCN) 2 in dilute THF solution (0.01
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::243753aa49123fe3ed8a7715f8e6557d
https://doi.org/10.1055/s-0030-1258560
https://doi.org/10.1055/s-0030-1258560
Autor:
Masashi Kawasaki, Chiho Hiraoka, Kanako Katayama, Naoki Toyooka, Akihisa Inoue, Akira Tanaka, Hiroko Kakuda, Michimasa Goto, Yuka Asano, Tadashi Kometani
Publikováno v:
Journal of Molecular Catalysis B: Enzymatic. 54:93-102
2-Substituted 4-chromanones were synthesized in their optically active forms. The chiral intermediates were obtained via lipase-catalyzed enantioselective reactions. Lipase and esterase were also used for the hydrolysis of ester moieties of the precu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::89126b7ffd6271506e76563c4b07a713
https://doi.org/10.1016/j.molcatb.2007.12.022
https://doi.org/10.1016/j.molcatb.2007.12.022
Autor:
Masayuki Kirihara, Hiroko Kakuda, Tatsuhiro Akimoto, Minori Morishita, Akihiko Hatano, Takuya Noguchi, Yoshiro Hirai, Akihiro Shimajiri
Publikováno v:
Tetrahedron Letters. 47:3777-3780
The reaction of tertiary cyclopropyl silyl ethers with diethylaminosulfur trifluoride in electron-rich aromatic compounds causes the Friedel–Crafts alkylation to produce allylated or cyclopropylated aromatic compounds.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc14fcbb7f91405b3d0677f8ea22a43c
https://doi.org/10.1016/j.tetlet.2006.03.120
https://doi.org/10.1016/j.tetlet.2006.03.120
Autor:
Michimasa Goto, Tadashi Kometani, Yuko Hayashi, Hiroko Kakuda, Masashi Kawasaki, Shigeki Kawabata, Naoki Toyooka, Akira Tanaka
Publikováno v:
Tetrahedron: Asymmetry. 16:4065-4072
The highly enantioselective kinetic resolution of a racemic primary alcohol by lipase-catalyzed transesterification with vinyl 3-(4-trifluoromethylphenyl)propanoate afforded an enantiomerically pure primary alcohol. The versatility of this approach i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7136d390522e32c9e85d0b68d257036e
https://doi.org/10.1016/j.tetasy.2005.10.041
https://doi.org/10.1016/j.tetasy.2005.10.041
Autor:
Fumito Okafuji, Yoshihiro Mori, Kanae Ohto, Hiroko Kakuda, Taku Nakano, Noriyoshi Masuoka, Yasumaru Hatanaka
Publikováno v:
Bulletin of the Chemical Society of Japan. 78:703-709
In a model system of a water-soluble hemin, tetrakis(4-methylpyridyl)porphinatoiron(III) pentachloride (FeTMPyPCl5), with 3-methyl-2-benzothiazolinone hydrazone (MBTH), superoxide anion radical (O2...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11f0db1af4964500093cb24befa8f2c8
https://doi.org/10.1246/bcsj.78.703
https://doi.org/10.1246/bcsj.78.703
Autor:
Mamiko Nagaoka, Hiroko Kakuda, Hiroshi Ochiai, Yuji Matsuya, Kazushige Sasaki, Naoki Toyooka, Nobuko Imanishi, Hideo Nemoto
Publikováno v:
The Journal of Organic Chemistry. 69:7989-7993
The synthesis and evaluation of antiviral activity of new furan-fused tetracyclic compounds are described. The syntheses were satisfactorily achieved on the basis of o-quinodimethane chemistry, using furan-containing benzocyclobutene derivatives as a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a85ae49898a43e77b53ecadab4620c4
https://doi.org/10.1021/jo0486995
https://doi.org/10.1021/jo0486995
Autor:
Hiroko Kakuda, Masayuki Kirihara
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 62:919-928
The reaction of tertiary cyclopropanol systems with hypervalent iodines in a protic solvent caused oxidative bond cleavage at C1-C2 and C2-C3 leading to alkenoic acids or their corresponding esters in high yields. In the cases of the compounds bearin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2305b414460f69c9053a2916444ec04d
https://doi.org/10.5059/yukigoseikyokaishi.62.919
https://doi.org/10.5059/yukigoseikyokaishi.62.919
Publikováno v:
Bulletin of the Chemical Society of Japan. 76:2353-2360
Systems with pentafluoroiodosylbenzene (PFIB) and hemin (FeTPPCl8Cl) in dichloromethane were adopted to study the activities of the model system using toluenes as substrates for P450 enzymes. The oxidation products were mainly corresponding benzyl al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::703b000054f0a3e1d81e556d9225fa49
https://doi.org/10.1246/bcsj.76.2353
https://doi.org/10.1246/bcsj.76.2353
Publikováno v:
Tetrahedron: Asymmetry. 14:1529-1534
2-Methylchroman-4-one and 2-phenylchroman-4-one were synthesized in optically active form. Their chiral intermediates were obtained via lipase-catalyzed enantioselective reactions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7efdc40984abe5cc16a3df50f240eebf
https://doi.org/10.1016/s0957-4166(03)00277-5
https://doi.org/10.1016/s0957-4166(03)00277-5