Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yuichi Kuboki"'
Publikováno v:
Chemical and Pharmaceutical Bulletin. 71:93-100
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73c4221f73a636b8c9f52709a4d70c75
https://doi.org/10.1248/cpb.c22-00555
https://doi.org/10.1248/cpb.c22-00555
Publikováno v:
RSC Advances. 10:37797-37799
Herein, we report a ring-opening 1,3-arylboration of aryl cyclopropanes using BCl3 in the presence of arene nucleophiles. Formal 1,3-oxy arylation and 1,3-amino arylation of the arylcyclopropane via one-pot derivatization of the installed boron group
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca2663dcfc31b439e046f96f9e9fe06c
https://doi.org/10.1039/d0ra08151e
https://doi.org/10.1039/d0ra08151e
Autor:
Yuichi Kuboki, Mitsuhiro Arisawa, Yoshifumi Ueyama, Reiya Ohta, Kenichi Murai, Nao Matsumoto, Hiromichi Fujioka, Tomohiro Maegawa, Hiroshi Aoyama
Publikováno v:
The Journal of Organic Chemistry. 83:6432-6443
Acetals are the most useful protecting groups for carbonyl functional groups. In addition to the role of protection, they can also be used as synthons of carbonyl functions. Previously, we developed a chemoselective deprotection and nucleophilic subs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::600a7da85297338be17b8222fb1cbfae
https://doi.org/10.1021/acs.joc.8b00675
https://doi.org/10.1021/acs.joc.8b00675
Autor:
Yasuyuki Koutani, Yuichi Kuboki, Yuki Yoshikawa, Reiya Ohta, Hiromichi Fujioka, Tomohiro Maegawa
Publikováno v:
Journal of Fluorine Chemistry. 201:1-6
A versatile and chemoselective route has been developed for the synthesis of aliphatic fluorinated methyl ethers (ROCH 2 R F ), specifically monofluoromethyl ethers (ROCH 2 F) and trifluoromethylthiomethyl ethers (ROCH 2 SCF 3 ), through pyridinium-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::caa01ad41f7cf22ac2ac10a337db5348
https://doi.org/10.1016/j.jfluchem.2017.07.007
https://doi.org/10.1016/j.jfluchem.2017.07.007
Autor:
Jun-Ichi Haruta, Kazuto Nunomura, Yuichi Kuboki, Kenichi Murai, Akira Asai, Kenta Hayami, Mitsuhiro Arisawa, Megumi Fumimoto, Hiromichi Fujioka, Katsumi Ohta, Bangzhong Lin
Publikováno v:
HETEROCYCLES. 103:511
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efde82b6ef0635b2a30a9678475b7741
https://doi.org/10.3987/com-20-s(k)35
https://doi.org/10.3987/com-20-s(k)35
Autor:
Kenichi Murai, Nao Matsumoto, Reiya Ohta, Hidenobu Mitsukane, T. Kimura, Yuichi Kuboki, Hiromichi Fujioka
Publikováno v:
CHEMICAL & PHARMACEUTICAL BULLETIN. 64:718-722
The intermediates formed during the Beckmann fragmentation of α-alkoxy and α-alkoxy-α-alkyl oxime acetates have been successfully trapped as phosphonium salts, which were subsequently reacted with a variety of Grignard reagents to give the corresp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e156ea1fed809eeb8859d57d4c21ea56
https://doi.org/10.1248/cpb.c16-00006
https://doi.org/10.1248/cpb.c16-00006
Autor:
Hiromichi, Fujioka, Nao, Matsumoto, Yuichi, Kuboki, Hidenobu, Mitsukane, Reiya, Ohta, Takashi, Kimura, Kenichi, Murai
Publikováno v:
Chemicalpharmaceutical bulletin. 64(7)
The intermediates formed during the Beckmann fragmentation of α-alkoxy and α-alkoxy-α-alkyl oxime acetates have been successfully trapped as phosphonium salts, which were subsequently reacted with a variety of Grignard reagents to give the corresp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::06c89adc13743d659db32f161289f528
https://pubmed.ncbi.nlm.nih.gov/27373627
https://pubmed.ncbi.nlm.nih.gov/27373627
Autor:
Reiya Ohta, Nao Matsumoto, Yoshifumi Ueyama, Yuichi Kuboki, Hiroshi Aoyama, Kenichi Murai, Mitsuhiro Arisawa, Tomohiro Maegawa, Hiromichi Fujioka
Publikováno v:
Journal of Organic Chemistry; 6/15/2018, Vol. 83 Issue 12, p6432-6443, 12p