A. Nishiguchi

Phosphine-Catalyzed Enantioselective Intramolecular [3+2] Annulations To Generate Fused Ring Systems

Y. Fujiwara, G. C. Fu, Sarah Yunmi Lee, 2015, Journal of the American Chemical Society.

A practical chromatography-free synthesis of a 5,6-dihydroimidazolo[1,5-f]pteridine derivative as a polo-like kinase-1 inhibitor

A. Nishiguchi, Osamu Yabe, K. Nakaoka, 2018, Tetrahedron.

Sulfonyl chloride formation from thiol derivatives by N-chlorosuccinimide mediated oxidation

A. Nishiguchi, K. Maeda, S. Miki, 2006 .

Convenient efficient synthesis of TAK-779, a nonpeptide CCR5 antagonist: development of preparation of various ammonium salts using trialkylphosphite and N-halogenosuccinimide

A. Nishiguchi, T. Ikemoto, M. Wakimasu, 2001 .

Hydroximate as a synthetically useful functional group: A novel synthesis of lactones using hydroximates as a tether

A. Nishiguchi, O. Miyata, T. Naito, 1996 .

Facile synthesis of 7–10 membered rings by intramolecular condensation using dialkylcarbonate as solvent

Tatsuya Ito, A. Nishiguchi, T. Ikemoto, 2004 .

Efficient synthesis of CCR5 antagonist, 2,3-dihydro-1-benzothiepine derivatives by improved intramolecular Claisen type reaction using dialkylcarbonate

Tatsuya Ito, A. Nishiguchi, T. Ikemoto, 2004 .