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Kouji Hattori

Observed names: K. HATTORI, K. Hattori
OpenAlex ID: A5111647376
A New Chiral BLA Promoter for Asymmetric Aza Diels-Alder and Aldol-Type Reactions of Imines
1994 · Kazuaki Ishihara, Mayumi Miyata, et al. · Journal of the American Chemical Society · 199
Asymmetric aza-Diels-Alder reaction: enantio- and diastereoselective reaction of imine mediated by Chiral Lewis acid
1993 · Kouji Hattori, Hisashi Yamamoto · Tetrahedron · 149
Asymmetric aza-Diels-Alder reaction mediated by chiral boron reagent
1992 · Kouji Hattori, Hisashi Yamamoto · The Journal of Organic Chemistry · 143
Highly selective and operationally simple synthesis of enantiomerically pure .beta.-amino esters via double stereodifferentiation
1993 · Kouji Hattori, Mayumi Miyata, et al. · Journal of the American Chemical Society · 133
Rational Approaches to Discovery of Orally Active and Brain-Penetrable Quinazolinone Inhibitors of Poly(ADP-ribose)polymerase
2004 · Kouji Hattori, Yoshiyuki Kido, et al. · Journal of Medicinal Chemistry · 100
Inhibitor‐induced structural change of the active site of human poly(ADP‐ribose) polymerase
2003 · Takayoshi Kinoshita, Isao Nakanishi, et al. · FEBS Letters · 98
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Discovery of potent and selective PARP-1 and PARP-2 inhibitors: SBDD analysis via a combination of X-ray structural study and homology modeling
2005 · Junya Ishida, Hirofumi Yamamoto, et al. · Bioorganic & Medicinal Chemistry · 87
A Novel and Potent Poly(ADP-Ribose) Polymerase-1 Inhibitor, FR247304 (5-Chloro-2-[3-(4-phenyl-3,6-dihydro-1(2 H)-pyridinyl)propyl]-4(3 H)-quinazolinone), Attenuates Neuronal Damage in in Vitro and in Vivo Models of Cerebral Ischemia
2004 · Akinori Iwashita, Nobuteru Tojo, et al. · Journal of Pharmacology and Experimental Therapeutics · 87
Discovery of quinazolinone and quinoxaline derivatives as potent and selective poly(ADP‐ribose) polymerase‐1/2 inhibitors
2005 · Akinori Iwashita, Kouji Hattori, et al. · FEBS Letters · 81
Highly selective generation and application of (E)- and (Z)-silyl ketene acetals from .alpha.-hydroxy esters
1993 · Kouji Hattori, Hisashi Yamamoto · The Journal of Organic Chemistry · 68
Neuroprotective Effects of a Novel Poly(ADP-Ribose) Polymerase-1 Inhibitor, 2-{3-[4-(4-Chlorophenyl)-1-piperazinyl] propyl}-4(3 H)-quinazolinone (FR255595), in an in Vitro Model of Cell Death and in Mouse 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Model of Parkinson’s Disease
2004 · Akinori Iwashita, Syunji Yamazaki, et al. · Journal of Pharmacology and Experimental Therapeutics · 67
Practical preparation of α-hydroxy-β-amino ester units; Stereoselective synthesis of taxol side chain and norstatine
1994 · Kouji Hattori, Hisashi Yamamoto · Tetrahedron · 65
Asymmetric Aza-Diels-Alder Reaction Catalyzed by Boron Reagent: Effect of Biphenol and Binaphthol Ligand
1993 · Kouji Hattori, Hisashi Yamamoto · Synlett · 54
Discovery of a Novel Series of Biphenyl Benzoic Acid Derivatives as Potent and Selective Human β3-Adrenergic Receptor Agonists with Good Oral Bioavailability. Part I
2008 · Masashi Imanishi, Yasuyo Tomishima, et al. · Journal of Medicinal Chemistry · 45
A New Poly(ADP-Ribose) Polymerase Inhibitor, FR261529 [2-(4-Chlorophenyl)-5-quinoxalinecarboxamide], Ameliorates Methamphetamine-Induced Dopaminergic Neurotoxicity in Mice
2004 · Akinori Iwashita, Kayoko Mihara, et al. · Journal of Pharmacology and Experimental Therapeutics · 42
4-Phenyl-1,2,3,6-tetrahydropyridine, an excellent fragment to improve the potency of PARP-1 inhibitors
2005 · Junya Ishida, Kouji Hattori, et al. · Bioorganic & Medicinal Chemistry Letters · 37
Highly selective enolization method for heteroatom substituted esters; its application to the ireland ester enolate claisen rearrangement
1994 · Kouji Hattori, Hisashi Yamamoto · Tetrahedron · 36
Rational design of conformationally restricted quinazolinone inhibitors of poly(ADP-ribose)polymerase
2007 · Kouji Hattori, Yoshiyuki Kido, et al. · Bioorganic & Medicinal Chemistry Letters · 34
Asymmetric synthesis of FR165914: A novel β3-adrenergic agonist with a benzocycloheptene structure
1995 · Kouji Hattori, Masanobu Nagano, et al. · Bioorganic & Medicinal Chemistry Letters · 34
Discovery of a Novel Series of Biphenyl Benzoic Acid Derivatives as Highly Potent and Selective Human β3 Adrenergic Receptor Agonists with Good Oral Bioavailability. Part II
2008 · Masashi Imanishi, Shinji Itou, et al. · Journal of Medicinal Chemistry · 30
A novel pyridazinone derivative as a nonprostanoid PGI2 agonist
2000 · Kazunori Tsubaki, Kiyoshi Taniguchi, et al. · Bioorganic & Medicinal Chemistry Letters · 23
Synthesis, SAR study, and biological evaluation of novel quinoline derivatives as phosphodiesterase 10A inhibitors with reduced CYP3A4 inhibition
2014 · Wataru Hamaguchi, Naoyuki Masuda, et al. · Bioorganic & Medicinal Chemistry · 22
Discovery of a Novel Series of Benzoic Acid Derivatives as Potent and Selective Human β 3 Adrenergic Receptor Agonists with Good Oral Bioavailability. 3. Phenylethanolaminotetraline (PEAT) Skeleton Containing Biphenyl or Biphenyl Ether Moiety
2008 · Masashi Imanishi, Yutaka Nakajima, et al. · Journal of Medicinal Chemistry · 21
Synthesis and antibacterial evaluation of novel 2-[N-Imidoylpyrrolidinyl] carbapenems
2002 · Kouji Hattori, Akira Yamada, et al. · Bioorganic & Medicinal Chemistry Letters · 19
Discovery of diphenylcarbamate derivatives as highly potent and selective IP receptor agonists: Orally active prostacyclin mimetics. Part 3
2005 · Kouji Hattori, Akira Tanaka, et al. · Bioorganic & Medicinal Chemistry Letters · 17
Works count: 58
Citation count: 1,841
H-index: 22
I10-index: 35
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