Takayuki Suzuki

发表

Structure–Activity Relationship and Rational Design of 3,4-Dephostatin Derivatives as Protein Tyrosine Phosphatase Inhibitors

Y. Umezawa, K. Umezawa, M. Otsuka, 2000 .

Discovery of novel thiourea derivatives as potent and selective beta3-adrenergic receptor agonists.

K. Onda, Takayuki Suzuki, T. Matsui, 2009, Bioorganic & medicinal chemistry.

Discovery of N-ethylpyridine-2-carboxamide derivatives as a novel scaffold for orally active γ-secretase modulators.

Takayuki Suzuki, Y. Mitani, H. Akashiba, 2019, Bioorganic & medicinal chemistry.

Chemoselective and Kilogram-Scale Synthesis of Acetanilide β3-Adrenergic Receptor Agonist

K. Onda, Takayuki Suzuki, M. Okada, 2015 .

An efficient synthesis of γ-amino β-ketoester by cross-claisen condensation with α-amino acid derivatives

Takayuki Suzuki, S. Katayama, K. Izawa, 2003 .

Synthetic study on aplysiatoxins, highly inflammatory agents and tumor promoters synthesis of the three optically active segments

Takayuki Suzuki, S. Nishiyama, S. Yamamura, 1989 .

Synthesis of optically active alpha-aminoalkyl alpha'-halomethyl ketone: a cross-Claisen condensation approach.

Takayuki Suzuki, S. Katayama, K. Izawa, 2002, Organic letters.

Stereoselective construction of cis-transoid-cis-tricyclo[7.3.0.0]dodecanes by an intramolecular Diels–Alder reaction: a formal total synthesis of (±)-Δ9(12)-capnellene

Takayuki Suzuki, M. Ihara, K. Fukumoto, 1992 .

A stereoselective total synthesis of (±)-Δ9(12)-capnellene via the intramolecular Diels–Alder approach

Takayuki Suzuki, M. Ihara, K. Fukumoto, 1991 .

New approaches to the industrial synthesis of HIV protease inhibitors.

Takayuki Suzuki, S. Katayama, K. Izawa, 2004, Organic & biomolecular chemistry.

Polymer-supported bases, 4. Macrolide synthesis from ω-bromocarboxylic acids using polymer-supported 1,8-diazabicyclo[5.4.0]undec-7-ene†

Takayuki Suzuki, M. Tomoi, Takashi Watanabe, 1985 .

Discovery of Ipragliflozin (ASP1941): a novel C-glucoside with benzothiophene structure as a potent and selective sodium glucose co-transporter 2 (SGLT2) inhibitor for the treatment of type 2 diabetes mellitus.

Atsushi Noda, Hiroshi Tomiyama, M. Takeuchi, 2012, Bioorganic & medicinal chemistry.

Synthetic studies on bryostatins, antineoplastic metabolites: Convergent synthesis of the C1-C16 fragment shared by all of the bryostatin family

K. Ohmori, Takayuki Suzuki, S. Nishiyama, 1993 .

An efficient synthesis of N-protected threo (2R,3S)-3-amino-1,2-epoxy phenylbutane

Takayuki Suzuki, K. Izawa, Y. Honda, 2005 .

Remarkable Diastereomeric Rearrangement of an α-Acyloxy β-Ketosulfide to an α-Acyloxy Thioester: A Novel Approach to the Synthesis of Optically Active (2S,3S) β-Amino α-Hydroxy Acids

Robert M. Williams, Takayuki Suzuki, K. Izawa, 2005 .

Synthesis and biological evaluation of C-glucosides with azulene rings as selective SGLT2 inhibitors for the treatment of type 2 diabetes mellitus: discovery of YM543.

Atsushi Noda, M. Takeuchi, Takayuki Suzuki, 2013, Bioorganic & medicinal chemistry.

Synthesis and phase-transfer catalytic activity of polymer-supported poly(ethylene glycol)s

Takayuki Suzuki, M. Tomoi, H. Kakiuchi, 1989 .

Synthesis and evaluation of N-phenyl-(2-aminothiazol-4-yl)acetamides with phenoxypropanolamine moiety as selective β3-adrenergic receptor agonists.

K. Onda, Takayuki Suzuki, T. Matsui, 2012, Chemical & pharmaceutical bulletin.

Synthesis and evaluation of novel phenylethanolamine derivatives containing acetanilides as potent and selective beta3-adrenergic receptor agonists.

K. Onda, Takayuki Suzuki, T. Matsui, 2010, Chemical & pharmaceutical bulletin.

Synthesis of 5-chloro-N-aryl-1H-indole-2-carboxamide derivatives as inhibitors of human liver glycogen phosphorylase a.

K. Onda, K. Negoro, K. Momose, 2008, Bioorganic & medicinal chemistry.