Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Shingo Fujioka"'
Autor:
Wataru Asano, Kenji Yamanaka, Yasunori Ohara, Toru Uhara, Satoki Doi, Takuya Orita, Tomoko Iwanaga, Tsuyoshi Adachi, Shingo Fujioka, Tatsuo Akaki, Kazutaka Ikegashira, Yoshiji Hantani
Publikováno v:
Biochemistry; 7/18/2023, Vol. 62 Issue 14, p2161-2169, 9p
Publikováno v:
Organic Letters. 7:5143-5146
[reaction, structure: see text] Conjugate addition of various prochiral nitroalkanes to cyclic alpha,beta-unsaturated ketones was found to be efficiently catalyzed by N-spiro C2-symmetric chiral quaternary ammonium bromide 1b possessing a 3,5-bis(3,4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9543e370dfb88c4566284588fe38ac9
https://doi.org/10.1021/ol0517170
https://doi.org/10.1021/ol0517170
Publikováno v:
Synlett. :1655-1658
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cffb00d59f36f59b8abb2227dbfd77c9
https://doi.org/10.1055/s-2003-41424
https://doi.org/10.1055/s-2003-41424
Autor:
Ryo Sudo, Toshihiro Mitaka, Roger D. Kamm, Seok Chung, Yamato Kikkawa, Shingo Fujioka, Kazuo Tanishita, Johann Kalchman
Publikováno v:
Springer-Verlag
Most anti-cancer drug screening assays are currently performed in two dimensions, on flat, rigid surfaces. However, there are increasing indications that three-dimensional (3D) platforms provide a more realistic setting to investigate accurate morpho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ca6fecf95c8748741613de37215496c
http://hdl.handle.net/1721.1/104639
http://hdl.handle.net/1721.1/104639
Publikováno v:
The Proceedings of the Bioengineering Conference Annual Meeting of BED/JSME. :83-84
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e9c1ab8e7d4927bbd28cc26d68c4192d
https://doi.org/10.1299/jsmebio.2014.26.83
https://doi.org/10.1299/jsmebio.2014.26.83
Publikováno v:
ChemInform. 32
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c857a6ef0adf7832d399add12251be6c
https://doi.org/10.1002/chin.200124035
https://doi.org/10.1002/chin.200124035
Publikováno v:
ChemInform. 35
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd6e87dd6ce926952c42e6bff2953ee3
https://doi.org/10.1002/chin.200401035
https://doi.org/10.1002/chin.200401035
Publikováno v:
Seibutsu Butsuri. 54:S301
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::207679cdf2e00213a130698a86d38ea7
https://doi.org/10.2142/biophys.54.s301_3
https://doi.org/10.2142/biophys.54.s301_3
Publikováno v:
Journal of the American Chemical Society. 126:11790-11791
Highly enantioselective conjugate addition of nitroalkanes to alkylidenemalonates has been accomplished for the first time by the utilization of efficient phase-transfer catalysis of N-spiro C2-symmetric chiral quaternary ammonium bromide 1. For inst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b14d2fcd230cfd553b664cb65a56e18e
https://doi.org/10.1021/ja047047v
https://doi.org/10.1021/ja047047v
Publikováno v:
Journal of the American Chemical Society. 126:9558-9559
Direct catalytic asymmetric Michael addition reactions of ketones to nitroolefins using newly developed chiral pyrrolidine-pyridine conjugate bases as catalysts are described. The desired 1,4-adducts are obtained in excellent yields with high enantio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d39bf67fb1cec9387d3f814c14d77cad
https://doi.org/10.1021/ja046871g
https://doi.org/10.1021/ja046871g