K. Wakasugi

发表

Novel and efficient method for esterification, amidation between carboxylic acids and equimolar amounts of alcohols, and amines utilizing Me2NSO2Cl and N,N-dimethylamines; its application to the synthesis of coumaperine, a natural chemopreventive dieneamide

A. Iida, Y. Tanabe, N. Nakatani, 2003 .

Novel and Efficient Method for Esterification, Amidation Between Carboxylic Acids and Equimolar Amounts of Alcohols, and Amines Utilizing Me2NSO2Cl and N,N‐Dimethylamines; Its Application to the Synthesis of Coumaperine (XII), a Natural Chemopreventive Dieneamide.

A. Iida, Y. Tanabe, N. Nakatani, 2003 .

Me2NSO2Cl and N,N-dimethylamines; a novel and efficient agent for esterification, amidation between carboxylic acids, and equimolar amounts of alcohols and amines

Y. Tanabe, K. Wakasugi, A. Nakamura, 2001 .

Diphenylammonium triflate (DPAT): efficient catalyst for esterification of carboxylic acids and for transesterification of carboxylic esters with nearly equimolar amounts of alcohols

Y. Tanabe, T. Misaki, K. Wakasugi, 2000 .

Synthesis of BACE1 Inhibitors E2609/E2071 via Oxime–Olefin Cycloaddition Following a Process Risk Mitigation Strategy

Yoichi Kita, M. Bracke, A. Chanda, 2021, Organic Process Research & Development.

Pentafluorophenylammonium triflate (PFPAT): an efficient, practical, and cost-effective catalyst for esterification, thioesterification, transesterification, and macrolactone formation

Y. Tanabe, T. Misaki, K. Wakasugi, 2006 .

Chirality exchange from sp3 central chirality to axial chirality: benzannulation of optically active diaryl-2,2-dichlorocyclopropylmethanols to axially chiral alpha-arylnaphthalenes.

Y. Tanabe, Y. Nishii, K. Wakasugi, 2004, Journal of the American Chemical Society.

Pentafluorophenylammonium triflate (PFPAT): an efficient, practical, and cost-effective catalyst for esterification, thioesterification, transesterification, and macrolactone formation

Y. Tanabe, T. Misaki, K. Wakasugi, 2006 .

Simple, Mild, and Practical Esterification, Thioesterification, and Amide Formation Utilizing p‐Toluenesulfonyl Chloride and N‐Methylimidazole

A. Iida, Y. Tanabe, T. Misaki, 2003 .

Regiocontrolled benzannulation of diaryl(gem-dichlorocyclopropyl)methanols for the synthesis of unsymmetrically substituted alpha-arylnaphthalenes: application to total synthesis of natural lignan lactones.

E. Yoshida, Y. Tanabe, J. Motoyoshiya, 2005, The Journal of organic chemistry.

Cyclopropane-shift type reaction of diaryl(2-halogenocyclopropyl)methanols promoted by Lewis acids

Y. Tanabe, Y. Nishii, K. Wakasugi, 2000 .

Stereoselective Bifurcating-type Radical Cyclization of gem-Dibromocyclopropanes for the Synthesis of Uniquely Fused 5-3-5-Type Tricyclic Compounds

K. Yanagi, Y. Tanabe, Y. Nishii, 2002 .

Synthesis and stereostructure-activity relationship of three asymmetric center pyrethroids: 2-methyl-3-phenylcyclopropylmethyl 3-phenoxybenzyl ether and cyanohydrin ester.

Y. Nishii, K. Wakasugi, N. Maruyama, 2001, Bioorganic & medicinal chemistry.

Dimethylation and Hydrodechlorination of gem-Dichlorocyclopropanes with Grignard Reagents Promoted by Fe(III) or Co(II) Catalyst

Y. Tanabe, Y. Nishii, K. Wakasugi, 1998 .

Simple, Mild, and Practical Esterification, Thioesterification, and Amide Formation Utilizing p-Toluenesulfonyl Chloride and N-Methylimidazole.

A. Iida, Y. Tanabe, T. Misaki, 2004 .