Zobrazeno 1 - 10
of 183
pro vyhledávání: '"Ikuzo Nishiguchi"'
Publikováno v:
Electroorganic Synthesis ISBN: 9780203758571
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::752e8e84f18805bba9a58475234d486b
https://doi.org/10.1201/9780203758571-45
https://doi.org/10.1201/9780203758571-45
Publikováno v:
Synlett. 23:401-404
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1aefcd3626f35b2a1a1185cf31a7f16
https://doi.org/10.1055/s-0031-1290325
https://doi.org/10.1055/s-0031-1290325
Autor:
Takeshi Miyazaki, Yoshimasa Yamamoto, Hirofumi Maekawa, Yoshiko Yamanaka, Ikuzo Nishiguchi, Kazuaki Yonemura
Publikováno v:
Tetrahedron. 67:1598-1602
Treatment of various types of aromatic δ-ketoesters 2, 7, and 9 with Mg-turnings for Grignard reaction at −5 to 0 °C in N,N-dimethylformamide (DMF) containing trimethylsilyl chloride (TMSCl) brought about selective and reductive intramolecular cy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02f682153a62bcf433b79190fcc476e3
https://doi.org/10.1016/j.tet.2010.12.030
https://doi.org/10.1016/j.tet.2010.12.030
Publikováno v:
Tetrahedron Letters. 51:796-799
Mg-promoted reduction of benzophenones in the presence of ethyl trifluoroacetate and trimethylchlorosilane in N-methyl-2-pyrrolidinone afforded the corresponding cross-coupling products, which were easily transformed into C-trifluoroacetylated compou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a77991b42f899d6c396e45b16bbe966a
https://doi.org/10.1016/j.tetlet.2009.11.110
https://doi.org/10.1016/j.tetlet.2009.11.110
Publikováno v:
Electrochemistry. 78:208-212
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6cbc38fc2f8a0ba3d37ce33a0a19653
https://doi.org/10.5796/electrochemistry.78.208
https://doi.org/10.5796/electrochemistry.78.208
Autor:
Ikuzo Nishiguchi
Publikováno v:
Journal of Synthetic Organic Chemistry, Japan. 68:824-833
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77b579fb723ff91495091b153dfa1b6c
https://doi.org/10.5059/yukigoseikyokaishi.68.824
https://doi.org/10.5059/yukigoseikyokaishi.68.824
Publikováno v:
ECS Transactions. 13:1-6
Anodic oxidation of polyfluorinated benzene and naphthalene derivatives(1) bearing 1,4-difluoro groups in a mixed solvent of trifluoroacetic acid and methylene dichloride brought about facile and selective formation of the corresponding polyfluoro-1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67766eec32bb3d9b045d06d5eee1fe7a
https://doi.org/10.1149/1.3010724
https://doi.org/10.1149/1.3010724
Publikováno v:
ECS Transactions. 6:1-7
Electroreductive of aromatic imine derivatives (1) with methyl trichloroacetate (2) in N,N-dimethylacetamide (DMAc) containing Et4NBr as a supporting electrolyte using an undivided cell equipped with Zn-plates as the electrodes under constant current
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abb5efe2a94130924977aa6230876ff9
https://doi.org/10.1149/1.2790394
https://doi.org/10.1149/1.2790394
Publikováno v:
ECS Transactions. 2:29-32
Electroreduction of benzoic anhydride derivatives in the presence of aliphatic acid anhydrides gave the corresponding C- and O-diacylated products or 1,2-diacetoxy olefins depending upon the reaction conditions. Particularly, nucleophilic acylation o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa8a328466cfae2b5e30819327896c3c
https://doi.org/10.1149/1.2409002
https://doi.org/10.1149/1.2409002
Autor:
Koji Yamamoto, Hirofumi Maekawa, Tetsuro Uchida, Shun-ichi Kametani, Ikuzo Nishiguchi, Goro Tsukamoto
Publikováno v:
YAKUGAKU ZASSHI. 126:179-186
A new type of S-protected thiol-type thiamines (prodrugs), which have a (5-methyl-2-oxo-1,3-dioxol-4-yl) methyl group recognized as a biologically safe promoiety, were designed, prepared, and confirmed to show higher serum thiamine levels after oral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::175bdf4559879b5213e773f57ae117ce
https://doi.org/10.1248/yakushi.126.179
https://doi.org/10.1248/yakushi.126.179