Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Hajime, Nitta"'
Autor:
Shunsuke Tamba, Masashi Nitani, Takuji Seo, Hajime Nitta, Hikaru Tanaka, Kazutake Hagiya, Yoshio Aso, Yutaka Ie
Publikováno v:
Organic Letters. 24:3792-3796
Autor:
Shunsuke, Tamba, Masashi, Nitani, Takuji, Seo, Hajime, Nitta, Hikaru, Tanaka, Kazutake, Hagiya, Yoshio, Aso, Yutaka, Ie
Publikováno v:
Organic letters. 24(21)
The incorporation of an electron-accepting unit into π-conjugated systems is an important approach to modulate the physical properties of such molecules. To investigate the potential of tetrazolo[1,5
Autor:
Motoyoshi Noike, Yusuke Ono, Yuji Araki, Ryo Tanio, Yusuke Higuchi, Hajime Nitta, Yoshimitsu Hamano, Tomonobu Toyomasu, Takeshi Sassa, Nobuo Kato, Tohru Dairi
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e42090 (2012)
Many clinically useful pharmaceuticals are semi-synthesized from natural products produced by actinobacteria and fungi. The synthetic protocols usually contain many complicated reaction steps and thereby result in low yields and high costs. It is the
Externí odkaz:
https://doaj.org/article/df1cc149159240dfa4e787f5d52cfc83
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :1793-1798
The azido lactone 8 was prepared in a highly stereoselective manner by introduction of an azide function to the lactone 6 derived from L-aspartic acid, and then was converted into (2S,3S)-3-amino-2-azido-4-hydroxybutanoic acid 4. Four-component conde
Autor:
Philipp Thiel, Nobuo Kato, Regina Preisig-Müller, Vijay Renigunta, Christian Ottmann, Jürgen Daut, Kristin Koschinsky, Yusuke Higuchi, Carolin Anders, Günter Schlichthörl, Junko Ohkanda, Hajime Nitta, Maria Bartel, Benjamin Schumacher
Publikováno v:
Chemistry & Biology, 20(4), 583-593. Cell Press
SummarySmall-molecule stabilization of protein-protein interactions is an emerging field in chemical biology. We show how fusicoccanes, originally identified as fungal toxins acting on plants, promote the interaction of 14-3-3 proteins with the human
Autor:
Tohru Dairi, Yoshimitsu Hamano, Yusuke Ono, Takeshi Sassa, Motoyoshi Noike, Yuji Araki, Yusuke Higuchi, Ryo Tanio, Tomonobu Toyomasu, Nobuo Kato, Hajime Nitta
Publikováno v:
PLoS ONE
PLoS ONE, Vol 7, Iss 8, p e42090 (2012)
PLoS ONE, Vol 7, Iss 8, p e42090 (2012)
Many clinically useful pharmaceuticals are semi-synthesized from natural products produced by actinobacteria and fungi. The synthetic protocols usually contain many complicated reaction steps and thereby result in low yields and high costs. It is the
Publikováno v:
The Journal of Organic Chemistry. 67:3499-3501
A novel Hantzsch 1,4-dihydropyridine derivative could function in an organic solvent-free solution, and thus it could function in biological systems. These functions can be accomplished through regeneration of the reduced form of nicotinamine adenine
Publikováno v:
ChemInform. 28
The azido lactone 8 was prepared in a highly stereoselective manner by introduction of an azide function to the lactone 6 derived from L-aspartic acid, and then was converted into (2S,3S)-3-amino-2-azido-4-hydroxybutanoic acid 4. Four-component conde
Publikováno v:
ChemInform. 31
Publikováno v:
Chemical and Pharmaceutical Bulletin. 40:858-863
Reaction of benzaldehyde (1a) with methyl acetoacetate (2) in the presence of morpholine (or piperidine) and AcOH in refluxing C6H6 yielded a new condensation product, 1, 5-dimethoxycarbonyl-2-methyl-4-morpholino (or piperidino)-6-phenyl-1, 3-cyclohe