Yuji Ishihara

Lewis acid mediated reactions of organocopper reagents. Entrainment in the conjugate addition to .alpha.,.beta.-unsaturated ketones, esters, and acids via the RCu.cntdot.BF3 system

Yoshinori Yamamoto, Sinichi Yamamoto, Hidetaka Yatagai et al. · The Journal of Organic Chemistry · 1982 · 227 citations

Novel Organocatalysts, Engineering, Biochemistry +14

T-226296: a novel, orally active and selective melanin-concentrating hormone receptor antagonist

Shiro Takekawa, Asano Asami, Yuji Ishihara et al. · European Journal of Pharmacology · 2002 · 201 citations · Full text

Functional Selectivity, Medicine, Hormonal Receptor +7

Stereo- and regiocontrol of acyclic systems via the lewis acid mediated reaction of allylic stannanes with aldehydes

Yoshinori Yamamoto, Hidetaka Yatagai, Yuji Ishihara et al. · Tetrahedron · 1984 · 171 citations

Cross-coupling Reaction, Engineering, Acyclic Systems +9

Lewis Acid-Promoted, Stereocontrolled, Gram Scale, Diels−Alder Cycloadditions of Electronically Matched 2-Pyrones and Vinyl Ethers:  The Critical Importance of Molecular Sieves and the Temperature of Titanium Coordination with the Pyrone

Gary H. Posner, Haiyan Dai, DJ Bull et al. · The Journal of Organic Chemistry · 1996 · 110 citations

Chemical Engineering, Titanium Coordination, Engineering +12

TAK-147, an acetylcholinesterase inhibitor, increases choline acetyltransferase activity in cultured rat septal cholinergic neurons

Koki Kato, Hitomi Hayako, Yuji Ishihara et al. · Neuroscience Letters · 1999 · 94 citations

Molecular Physiology, Acetylcholinesterase Inhibitor, Biochemistry +7