Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Ken Ichi Ichikawa"'
1
Akademický článek
Dynamic planar scintigraphy for the rapid kinetic measurement of myocardial 123I-MIBG turnover can identify Lewy body disease
Autor: Yoshitaka Kumakura, Yuji Shimizu, Masatsugu Hariu, Ken-ichi Ichikawa, Norihito Yoshida, Masato Suzuki, Satoru Oji, Shinya Narukawa, Haruo Yoshimasu, Kyoichi Nomura
Publikováno v: EJNMMI Research, Vol 11, Iss 1, Pp 1-12 (2021)
Abstract Background Using two static scans for 123I-meta-iodobenzyl-guanidine (123I-MIBG) myocardial scintigraphy ignores the dynamic response from vesicular trapping in nerve terminals. Moreover, the long pause between scans is impractical for patie
Externí odkaz: https://doaj.org/article/7978b9caea2d4e70a5836932cc464c80
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2
Enantioselective addition of diethylzinc to aldehydes catalyzed by (R)-1-phenylethylamine-derived 1,4-amino alcohols
Autor: Naomichi Miyairi, Ken Ichi Ichikawa, Naoya Hosoda, Suguru Ito, Yukihiro Sasahara, Masatoshi Asami
Publikováno v: Tetrahedron. 71:6796-6802
A series of o-xylylene-type 1,4-amino alcohols, synthesized from (R)-1-phenylethylamine, were used as chiral ligands for the enantioselective addition of diethylzinc to benzaldehyde. (S)-1-Phenyl-1-propanol was obtained with high enantioselectivity i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6ab1638a01422f8fae400fbafb3baf8f
https://doi.org/10.1016/j.tet.2015.07.031
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3
Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by Diastereomeric 1,4-Amino Alcohols with o-Xylylene Skeleton
Autor: Suguru Ito, Naoya Hosoda, Ken Ichi Ichikawa, Atsushi Nagai, Masatoshi Asami, Yukihiro Sasahara
Publikováno v: Chemistry Letters. 44:345-347
Two diastereomeric 1,4-amino alcohols with o-xylylene structure (S,R)-2 and (S,S)-3, synthesized from chiral 1,4-diol (S,S)-1, were utilized as chiral ligands for the enantioselective addition of d...
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5c5877cdf683e138766b16cf45c47bea
https://doi.org/10.1246/cl.141113
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ChemInform Abstract: Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by (R)-1-Phenylethylamine-Derived 1,4-Amino Alcohols
Autor: Masatoshi Asami, Ken Ichi Ichikawa, Suguru Ito, Naoya Hosoda, Yukihiro Sasahara, Naomichi Miyairi
Publikováno v: ChemInform. 46
A series of o-xylylene-type 1,4-amino alcohols, synthesized from (R)-1-phenylethylamine, were used as chiral ligands for the enantioselective addition of diethylzinc to benzaldehyde. (S)-1-Phenyl-1-propanol was obtained with high enantioselectivity i
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::731b69936484a9a977e754e7ba19fa34
https://doi.org/10.1002/chin.201552045
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5
ChemInform Abstract: Enantioselective Addition of Diethylzinc to Aldehydes Catalyzed by Diastereomeric 1,4-Amino Alcohols with o-Xylylene Skeleton
Autor: Suguru Ito, Atsushi Nagai, Naoya Hosoda, Yukihiro Sasahara, Masatoshi Asami, Ken Ichi Ichikawa
Publikováno v: ChemInform. 46
Two diastereomeric 1,4-amino alcohols with o-xylylene structure (S,R)-2 and (S,S)-3, synthesized from chiral 1,4-diol (S,S)-1, were utilized as chiral ligands for the enantioselective addition of d...
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e33d65860ba0c919b935fab7820c44a9
https://doi.org/10.1002/chin.201536070
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9
Akademický článek
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