A. Ohno

发表

A simple and practical method for the stereoselective synthesis of (Z)-1-iodo-1-alkenes from 1,1-diiodo-1-alkenes

Yoshinori Yamamoto, I. Kadota, H. Ueno, 2003 .

Synthesis of the H ring of gambierol

Yoshinori Yamamoto, I. Kadota, Y. Matsukawa, 1998 .

Convergent synthesis of polycyclic ethers via the intramolecular allylation of alpha-acetoxy ethers and subsequent ring-closing metathesis: synthesis of the CDEFG ring system of gambierol.

I. Kadota, Y. Yamamoto, A. Ohno, 2001, Journal of the American Chemical Society.

Practical Syntheses of EnantiomericallyPure Key Intermediates of Opioid Receptor-like 1 (ORL1)Antagonists

H. Kigoshi, O. Okamoto, T. Yoshizumi, 2009 .

Total synthesis of gambierol.

Yoshinori Yamamoto, Hiroyoshi Takamura, I. Kadota, 2003, Journal of the American Chemical Society.

Regioselective synthesis of 1,3,5-unsymmetrically substituted benzenes via the palladium-catalyzed cyclotrimerization of 1,3-diynes

Yoshinori Yamamoto, V. Gevorgyan, I. Kadota, 1997 .

Synthesis and biological evaluation of imidazole derivatives as novel NOP/ORL1 receptor antagonists: exploration and optimization of alternative pyrazole structure.

S. Ozaki, H. Ohta, Kensuke Kobayashi, 2009, Bioorganic & medicinal chemistry letters.

Convergent total syntheses of gambierol and 16-epi-gambierol and their biological activities.

M. Satake, Yoshinori Yamamoto, Hiroyoshi Takamura, 2003, Journal of the American Chemical Society.

A Simple and Practical Method for the Stereoselective Synthesis of (Z)-1-Iodo-1-alkenes from 1,1-Diiodo-1-alkenes.

Yoshinori Yamamoto, I. Kadota, H. Ueno, 2004 .

Convergent synthesis of polycyclic ethers via the intramolecular allylation of alpha-acetoxy ethers and subsequent ring-closing metathesis.

Yoshinori Yamamoto, I. Kadota, A. Ohno, 2002, Journal of the American Chemical Society.

Discovery and structure-activity relationships of a novel class of quinazoline glucokinase activators.

M. Chiba, K. Kamata, M. Mitsuya, 2009, Bioorganic & medicinal chemistry letters.

2-Cyclohexylcarbonylbenzimidazoles as potent, orally available and brain-penetrable opioid receptor-like 1 (ORL1) antagonists.

Hisashi Ohta, Hiroshi Kawamoto, Satoshi Ozaki, 2009, Bioorganic & medicinal chemistry letters.

2-Cyclohexylcarbonylbenzimidazoles as potent, orally available and brain-penetrable opioid receptor-like 1 (ORL1) antagonists.

S. Ozaki, Y. Ishii, S. Ito, 2009, Bioorganic & medicinal chemistry letters.