Kenji. Suzuki

发表

Acetic acid-catalyzed diketopiperazine synthesis.

Kenji. Suzuki, Y. Sasaki, N. Endo, 1981 .

Synthesis and structure-affinity relationships of novel N-(1-ethyl-4-methylhexahydro-1,4-diazepin-6-yl)pyridine-3-carboxamides with potent serotonin 5-HT3 and dopamine D2 receptor antagonistic activity.

Hiroshi Harada, Shiro Kato, Naoyuki Yoshida, 2003, Journal of medicinal chemistry.

Synthesis and antibacterial activity of a novel series of potent DNA gyrase inhibitors. Pyrazole derivatives.

K. Nagai, N. Iwai, M. Wachi, 2004, Journal of medicinal chemistry.

Direct synthesis of novel 2-imino-1,3-selenazolidine derivatives from O-methanesulfonyl β-amino alcohol hydrochlorides

Kenji. Suzuki, N. Watanabe, H. Terauchi, 2005 .

Structure-activity relationship study of BACE1 inhibitors possessing a chelidonic or 2,6-pyridinedicarboxylic scaffold at the P(2) position.

Y. Kiso, Y. Hamada, S. Ishiura, 2014, Bioorganic & medicinal chemistry letters.

Novel BACE1 inhibitors possessing a 5-nitroisophthalic scaffold at the P2 position.

Y. Kiso, Y. Hamada, S. Ishiura, 2012, Bioorganic & medicinal chemistry letters.

Controlling the number and positions of oligonucleotides on gold nanoparticle surfaces.

K. Hosokawa, M. Maeda, Kenji. Suzuki, 2009, Journal of the American Chemical Society.

Species differences between human and rat in the substrate specificity of cathepsin K.

Kenji. Suzuki, K. Gohda, N. Teno, 2008, Journal of biochemistry.

Discovery of a novel and potent human and rat beta3-adrenergic receptor agonist, [3-[(2R)-[[(2R)-(3-chlorophenyl)-2-hydroxyethyl]amino]propyl]-1H-indol-7-yloxy]acetic acid.

Hitoshi Kawashima, S. Kato, Kenji. Suzuki, 2005, Chemical & pharmaceutical bulletin.

Novel and potent human and rat beta3-adrenergic receptor agonists containing substituted 3-indolylalkylamines.

Hitoshi Kawashima, S. Kato, Kenji. Suzuki, 2003, Bioorganic & medicinal chemistry letters.

Isolation of a New Antibiotic, Alaremycin, Structurally Related to 5-Aminolevulinic Acid from Streptomyces sp. A012304

K. Nagai, N. Iwai, M. Wachi, 2005, Bioscience, biotechnology, and biochemistry.

Construction of pyrrolophenanthridinone scaffolds mediated by samarium(II) diiodide and access to natural product synthesis

Kenji. Suzuki, M. Yamashita, M. Ozeki, 2015 .

Analysis of the components of Paeonia radix by capillary zone electrophoresis

Kenji. Suzuki, S. Honda, K. Kakehi, 1990 .

Ag(core)-AgCl(shell) standard microelectrode-loaded TiO2.

H. Tada, Kenji. Suzuki, T. Kawahara, 2007, Chemical communications.

Synthesis and biological properties of quaternized N-methylation analogs of D-Arg-2-dermorphin tetrapeptide

Kenji. Suzuki, Y. Sasaki, A. Ambo, 1994 .

Synthesis and antimicrobial activity of β-carboline derivatives with N2-alkyl modifications.

Kaori Tanaka, Kenji. Suzuki, M. Koketsu, 2018, Bioorganic & medicinal chemistry letters.

Accelerating effect of meta substituents in the ester-mediated nucleophilic aromatic substitution reaction

Kenji. Suzuki, N. Koike, S. Miyano, 1998 .

Discovery of Carbono(di)thioates as Indoleamine 2,3-Dioxygenase 1 Inhibitors.

K. Matsuno, A. Asai, O. Takikawa, 2021, ACS medicinal chemistry letters.

A mild and convenient method for the preparation of methylthiomethyl ethers: Protection of hydroxyl groups.

Kenji. Suzuki, J. Inanaga, M. Yamaguchi, 1979 .

Syntheses and properties of the major hydroxy metabolites in humans of blonanserin AD-5423, a novel antipsychotic agent.

H. Toda, Kenji. Suzuki, M. Sakamoto, 2005, Bioorganic & medicinal chemistry letters.

Design, synthesis and structure-activity relationship studies of novel indazole analogues as DNA gyrase inhibitors with Gram-positive antibacterial activity.

K. Nagai, M. Wachi, Kenji. Suzuki, 2004, Bioorganic & medicinal chemistry letters.

Synthesis and antibacterial activity of novel and potent DNA gyrase inhibitors with azole ring.

K. Nagai, M. Wachi, Kenji. Suzuki, 2004, Bioorganic & medicinal chemistry.

Synthesis of β-Alanine-containing Analogs of Bradykinin

Kenji. Suzuki, T. Abiko, 1966 .

4,5-dialkylsubstituted 2-imino-1,3-thiazolidine derivatives as potent inducible nitric oxide synthase inhibitors.

Kenji. Suzuki, M. Matsumoto, H. Terauchi, 2004, Bioorganic & medicinal chemistry.

Chiral 1,1'-binaphthyl-2,2'-diammonium salt catalysts for the enantioselective Diels-Alder reaction with alpha-acyloxyacroleins.

K. Nakano, A. Sakakura, K. Ishihara, 2006, Organic letters.

Potent DNA gyrase inhibitors; novel 5-vinylpyrazole analogues with Gram-positive antibacterial activity.

M. Wachi, Kenji. Suzuki, K. Ofuji, 2004, Bioorganic & medicinal chemistry letters.

A FORMAL TOTAL SYNTHESIS OF (±)-QUADRONE

T. Imanishi, Kenji. Suzuki, M. Yamashita, 1985 .

Indole synthesis from N-allenyl-2-iodoanilines under mild conditions mediated by samarium(II) diiodide.

Kenji. Suzuki, M. Yamashita, M. Ozeki, 2014, Organic & biomolecular chemistry.

Phosphono Nucleoside. Part 1. Synthesis of 2,3′-Anhydro-l′-deoxy-l′- phosphono- l-β-D-fructofuranosyl Uracil.

Kenji. Suzuki, T. Tatsuoka, K. Imao, 1986 .

Practical synthesis of (3S,4S)-3-methoxy-4-methylaminopyrrolidine

Kenji. Suzuki, K. Chiba, Kazuhiro Mizuno, 2001 .

The .BETA.-p-nitrobenzyl ester to minimize side reaction during treatment of aspartyl peptides with methanesulfonic acid.

Kenji. Suzuki, N. Endo, 1978 .

Molecular Structure and Mutual Recognition Between Host and Guest Molecules Found in the Crystal Structures of Oxacalix[4]arenes Complexed with Xylene Isomers

I. Nakanishi, K. Tomita, Kenji. Suzuki, 2000 .

The β-Phenacyl and β-p-Nitrobenzyl Esters to Suppress Side Reactions during Treatment of Aspartyl Peptides with Hydrogen Fluoride

K. Nitta, Kenji. Suzuki, Y. Sasaki, 1976 .

X-Ray crystal structure of p-isopropyldihomooxacalix[4]arene―o-xylene (1:1) complex

S. Fujii, K. Tomita, Z. Asfari, 1991 .

Excess enthalpies of o- and m-dihalogenated benzene+methyl methyl thiomethyl sulfoxide, +dimethyl su

Kenji. Suzuki, S. Takagi, Takayoshi Kimura, 1997 .

Thermodynamics of Liquid Mixtures Containing Methyl Methylthiomethyl Sulfoxide.

Kenji. Suzuki, S. Takagi, Takayoshi Kimura, 1990 .

Structure of p-tert-butylhexahomotrioxacalix[3]arene

Y. Yamagata, S. Fujii, K. Tomita, 1992 .

Napthalimidobenzamide DB-51630: a novel DNA binding agent inducing p300 gene expression and exerting a potent anti-cancer activity.

Y. Sugimoto, H. Nagasawa, K. Wierzba, 2005, Bioorganic & medicinal chemistry.

The crystal structure of N 1‐[2‐(2‐amino‐ethylamino)‐ethyl]‐ethane‐1,2‐diamine (polyamines) binding to the minor groove of d(CGCGCG)2, hexamer at room temperature

A. Rich, T. Hakoshima, Kenji. Suzuki, 2002, FEBS letters.

Electron spin resonance study of the formation of anion radicals over titanium exchanged Y-zeolite

Y. Ono, Kenji. Suzuki, T. Keii, 1974 .

OP0595, a new diazabicyclooctane: mode of action as a serine β-lactamase inhibitor, antibiotic and β-lactam 'enhancer'.

D. Livermore, T. Ida, Kenji. Suzuki, 2015, The Journal of antimicrobial chemotherapy.

Aromatic Hydroxylation with an Iron(III)–Catechol–H2O2 System. Mechanistic Implication of the Role of Catechol

Kenji. Suzuki, W. Tagaki, S. Tamagaki, 1989 .

Phosphononucleoside 1. synthesis of 2 3' anhydro 1' deoxy 1' phosphono 1 beta d fructofuranosyluracil

Kenji. Suzuki, T. Tatsuoka, K. Imao, 1986 .

Insulin Peptides. VII. The Synthesis of Two Decapeptide Derivatives Containing the C-Terminal Sequence of the B-Chain of Insulin

Kenji. Suzuki, P. Katsoyannis, 1963 .

Insulin Peptides. X. The Synthesis of the B-Chain of Insulin and Its Combination with Natural or Synthetis A-Chin to Generate Insulin Activity

Kenji. Suzuki, P. Katsoyannis, A. Tometsko, 1964 .

Fe(III)-catalyzed hydroxylation of benzene with H2O2 in the presence of quinones

Kenji. Suzuki, W. Tagaki, S. Tamagaki, 1983 .

IRON(III)‐CATALYZED HYDROXYLATION OF BENZENE WITH HYDROGEN PEROXIDE IN THE PRESENCE OF QUINONES

Kenji. Suzuki, W. Tagaki, S. Tamagaki, 1984 .

Solid-phase synthesis and opioid activities of [D-Ala2]deltorphin II analogs

Kenji. Suzuki, Y. Sasaki, A. Ambo, 1993 .

Discovery of a Novel and Potent Human and Rat β3‐Adrenergic Receptor Agonist, [3‐[(2R)‐[ [(2R)‐(3‐Chlorophenyl)‐2‐hydroxyethyl]amino]propyl]‐1H‐indol‐7‐yloxy] acetic Acid.

Hitoshi Kawashima, S. Kato, Kenji. Suzuki, 2005 .

Suppression of Diketopiperazine Formation in Solid Phase Peptide Synthesis

K. Nitta, Kenji. Suzuki, N. Endo, 1975 .

Lipophilic sulfonic acids as the phase transfer catalysts in the hydrolysis of p-nitrophenyl acetate

Kenji. Suzuki, N. Iwamoto, W. Tagaki, 1981 .

Novel and orally bioavailable inducible nitric oxide synthase inhibitors: synthesis and evaluation of optically active 4,5-dialkyl-2-iminoselenazolidine derivatives.

Kenji. Suzuki, M. Matsumoto, H. Minato, 2005, Bioorganic & medicinal chemistry letters.

Synthesis of possible metabolites of chlorpromazine. II. 3-, 8- and 9-hydroxychlorpromazine†‡

S. Nishibe, Kenji. Suzuki, A. A. Manian, 1968 .

Novel BACE1 inhibitors with a non-acidic heterocycle at the P1' position.

Y. Kiso, Y. Hamada, J. Nguyen, 2013, Bioorganic & medicinal chemistry.

Species differences between human and rat in the substrate specificity of cathepsin K.

Kenji. Suzuki, K. Gohda, N. Teno, 2008, Journal of biochemistry.

Direct Synthesis of Novel 2-Imino-1,3-selenazolidine Derivatives from O-Methanesulfonyl β-Amino Alcohol Hydrochlorides.

Kenji. Suzuki, N. Watanabe, H. Terauchi, 2005 .