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Tai Shiraishi
Institution:
Ono Pharmaceutical (Japan)
Observed institutions:
Tohoku University,
Ono Pharmaceutical (Japan)
OpenAlex ID:
A5112445800
Asymmetric Michael Addition of Malonate Anions to Prochiral Acceptors Catalyzed by l -Proline Rubidium Salt
1996
·
Masahiko Yamaguchi
, Tai Shiraishi
, et al.
·
The Journal of Organic Chemistry
·
261
A Catalytic Enantioselective Michael Addition of a Simple Malonate to Prochiral α,β‐Unsaturated Ketoses and Aldehydes
1993
·
Masahiko Yamaguchi
, Tai Shiraishi
, et al.
·
Angewandte Chemie International Edition in English
·
182
Asymmetric Michael addition of nitroalkanes to prochiral acceptors catalyzed by proline rubidium salts
1997
·
Masahiko Yamaguchi
, Yoshihiro Igarashi
, et al.
·
Tetrahedron
·
124
Catalytic asymmetric Michael addition of nitroalkane to enone and enal
1994
·
Masahiko Yamaguchi
, Tai Shiraishi
, et al.
·
Tetrahedron Letters
·
116
Eine katalytische enantioselektive Michael‐Addition eines Malonats an prochirale α,β‐ungesättigte Aldehyde und Ketone
1993
·
Masahiko Yamaguchi
, Tai Shiraishi
, et al.
·
Angewandte Chemie
·
50
Design and synthesis of a highly selective EP4-receptor agonist. part 1: 3,7-dithiaPG derivatives with high selectivity
2001
·
Toru Maruyama
, Masaki Asada
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
31
An Improved Synthesis of the Selective EP4 Receptor Agonist ONO-4819
2009
·
Chisa Ohta
, Shin-itsu Kuwabe
, et al.
·
The Journal of Organic Chemistry
·
23
Design and synthesis of a selective EP4-receptor agonist. Part 4: practical synthesis and biological evaluation of a novel highly selective EP4-receptor agonist
2002
·
Toru Maruyama
, Shin-Itsu Kuwabe
, et al.
·
Bioorganic & Medicinal Chemistry
·
23
Design and synthesis of a highly selective EP4-receptor agonist. Part 2: 5-thia and 9β-haloPG derivatives with improved stability
2001
·
Toru Maruyama
, Masaki Asada
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
16
Design and Synthesis of a Selective EP4-Receptor Agonist. Part 2: 3,7-DithiaPGE1 Derivatives with High Selectivity
2002
·
Toru Maruyama
, Masaki Asada
, et al.
·
Bioorganic & Medicinal Chemistry
·
14
Design and synthesis of a selective EP4-Receptor agonist. Part 1: discovery of 3,7-DithiaPGE1 derivatives and identification of Their ω chains
2002
·
Toru Maruyama
, Masaki Asada
, et al.
·
Bioorganic & Medicinal Chemistry
·
8
The Effect of Water and Phenol on the Chiral Oxazaborolidine-Catalyzed Reduction of a Prostaglandin Enone Derivative
2009
·
Chisa Ohta
, Shin-itsu Kuwabe
, et al.
·
Organic Process Research & Development
·
6
An Improved Synthesis of the Selective EP4 Receptor Agonist ONO-4819
2009
·
Chisa Ohta
, Shin-itsu Kuwabe
, et al.
·
The Journal of Organic Chemistry
·
1
ChemInform Abstract: Design and Synthesis of a Selective EP4‐Receptor Agonist. Part 3. 16‐Phenyl‐5‐thiaPGE1 and 9‐β‐Halo Derivatives with Improved Stability.
2002
·
Toru Maruyama
, Masaki Asada
, et al.
·
ChemInform
ChemInform Abstract: Design and Synthesis of a Selective EP4‐Receptor Agonist. Part 1. Discovery of 3,7‐DithiaPGE1 Derivatives and Identification of Their ω Chains.
2002
·
Toru Maruyama
, Masaki Asada
, et al.
·
ChemInform
ChemInform Abstract: Design and Synthesis of a Selective EP4‐Receptor Agonist. Part 2. 3,7‐DithiaPGE1 Derivatives with High Selectivity.
2002
·
Toru Maruyama
, Masaki Asada
, et al.
·
ChemInform
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Works count:
16
Citation count:
855
H-index:
10
I10-index:
10
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