Takaaki Araki

发表

Modification of protein with BGL 06 , a novel branched oligoglycerol derivative

M. Yamasaki, T. Suzawa, H. Yamaguchi, 2008 .

A practical synthesis of the PPARα agonist, (R)-K-13675, starting from (S)-2-hydroxybutyrolactone

Takaaki Araki, K. Shibuya, Y. Yamazaki, 2008 .

Design and synthesis of highly potent and selective human peroxisome proliferator-activated receptor alpha agonists.

B. Staels, J. Fruchart, Takaaki Araki, 2007, Bioorganic & Medicinal Chemistry Letters.

Design and synthesis of highly potent and selective human peroxisome proliferator-activated receptor alpha agonists.

B. Staels, J. Fruchart, Keisuke Inoue, 2007, Bioorganic & medicinal chemistry letters.

Improved performance by replacing iminodiacetic residues with glyceryl residues in symmetrically branched oligoglycerols.

H. Hattori, M. Yamasaki, Takaaki Araki, 2011, Bioorganic & medicinal chemistry letters.

A Quantitative Investigation of the Water‐Solubilizing Properties of Branched Oligoglycerols

T. Hino, Takaaki Araki, Masaki Kamiya, 2007 .

Diastereoselective intramolecular carbamoylketene/alkene [2 + 2] cycloaddition: enantioselective access to pyrrolidinoindoline alkaloids.

Masahiro Yoshida, K. Shishido, Takaaki Araki, 2013, Organic letters.

Enantioselective total syntheses of pygmaeocins B and C.

Masahiro Yoshida, K. Shishido, Y. Manabe, 2013, Organic letters.

Synthesis of a water-soluble molecular tweezer and a recognition study in an aqueous media

Tomoaki Kawano, N. Miyoshi, M. Shibuya, 2005 .

Novel Synthesis of Butyl (S)-2-Hydroxybutanoate, the Key Intermediate of PPARα Agonist (R)-K-13675 from Butyl (2S,3R)-Epoxybutanoate and Butyl (S)-2,3-Epoxypropanoate

Takaaki Araki, K. Shibuya, Y. Yamazaki, 2013 .