S. Hirano

Synthesis and biological evaluation of 1,2,3,4-tetrahydroisoquinoline derivatives as potent and selective M2 muscarinic receptor antagonists.

T. Shibanuma, T. Watanabe, I. Kinoyama, 1999, Chemical & pharmaceutical bulletin.

Synthesis and biological evaluation of phenylacetyl derivatives having low central nervous system permeability as potent and selective M2 muscarinic receptor antagonists.

A. Kakefuda, A. Tanaka, H. Shibata, 1998, Chemical & pharmaceutical bulletin.

Synthesis of novel succinamide derivatives having the 5,11-dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one skeleton as potent and selective M2 muscarinic receptor antagonists. I.

A. Kakefuda, H. Shibata, T. Watanabe, 1997, Chemical & pharmaceutical bulletin.

Development and Scale-Up of an Asymmetric Synthesis Process for Alogliptin

Ken-ichiro D Uno, M. Takasuga, R. Tsuruoka, 2021 .

Discovery of 4-Piperazine Isoquinoline Derivatives as Potent and Brain-Permeable Tau Prion Inhibitors with CDK8 Activity.

Benjamin C. Tang, Roy J. Vaz, Nick A. Paras, 2020, ACS medicinal chemistry letters.

Fluoreno[2,3-b]fluorene vs Indeno[2,1-b]fluorene: Unusual Relationship between the Number of π Electrons and Excitation Energy in m-Quinodimethane-Type Singlet Diradicaloids.

M. Nakano, T. Takui, R. Kishi, 2017, The Journal of organic chemistry.

Detection of active methylene compounds having cyano and carbonyl groups with chemiluminescent reaction using tris(2,2′-bipyridine)ruthenium(III) prepared by on-line electrochemical oxidation

K. Yokota, A. Muromatsu, S. Yamazaki, 1999 .