Session Details

[28-61-pm2]Chemical reaction development, mechanistic analysis, computational chemistry 11

Sat. Mar 28, 2026 3:30 PM - 5:30 PM JST
Sat. Mar 28, 2026 6:30 AM - 8:30 AM UTC
Room 61 (4201, Bldg. 4, Area 4 [2F]) (4)
Discusser: Keita Komine, Yuji Sumii

[28-61-pm2-27]Synthesis and molecular structure of diaryltellurides with hypervalent bond between tellurium and nitrogen atoms

○Mio Matsumura1, Ginga Sato1, Sohei Daiba1, Yuki Murata1, Shuji Yasuike1 (1. Sch. Pharm. Sci., Aichi Gakuin Univ.)

[28-61-pm2-28]Enhancement of copper–carbene insertion reactions by the tripodal ligand : oxa-TriQuinoline (o-TQ)

○Toi Kobayashi1, Naoya Kumagai1,2 (1. Grad. Sch. Pharm. Sci., Keio Univ., 2. Inst. Microb. Chem.)

[28-61-pm2-29S]Deep-Red to Near-Infrared Light-Driven Radical Generation from Organoboron Compounds via Ligand-Induced Direct Excitation Catalysis

○Kanji Muraoka1, Yusuke Miyamoto1, Sho Murakami2, Hirohisa Ohmiya2 (1. Grad. Sch. Pharm. Sci., Kyoto Univ., 2. Grad. Sch. Eng., Kyoto Univ.)

[28-61-pm2-30S]Asymmetric Michael reaction using fluorous cobalt salen complex

○Nina Gotoh1, Asahi Fujino1, Yuki Sawano2, Takayuki Shioiri1,2, Masato Matsugi1,2 (1. Grad. Sch. Agric., Meijo Univ., 2. Fac. Agric., Meijo Univ.)

[28-61-pm2-31S]Samarium-Catalyzed Redox-Neutral Cross-Pinacol Coupling Reaction

○Ayahito Kaneki1, Katsuma Ando1, Takahito Kuribara1, Tetsuhiro Nemoto1 (1. Grad. Sch. Pharm. Sci., Chiba Univ.)

[28-61-pm2-32S]Development of a bottom-up cubane synthesis method for introducing diverse substituents.

○Hinata Mimaki1, Masaru Tanioka1, Tsuyoshi Yamada1, Yuji Matsuya1 (1. Faculty of Pharm. Sci., University of Toyama)

[28-61-pm2-33]Cross-coupling reactions with heterogeneous catalysts prepared by flame spray pyrolysis

○Shintaro Kamio1, Tomoyuki Hirano2, Pham Van Tung2, Takehiro Yamagishi1, Takashi Ogi2 (1. Faculty of Pharmaceutical Scienses, Hokkaido University of Science, 2. Chemical Engineering Program, Department of Advanced Science and Engineering, Graduate School of Advanced Science and Engineering, Hiroshima University)

[28-61-pm2-34S]Development of an asymmetric [2+2+2] cycloaddition reaction of 1,6-diynes and alkenes using a Cobalt/Photoredox cooperative catalyst

○Rinto Fujii1, Keiji Yamada1, Yuki Ishikawa1, Kotoko Nakagawa1, Takeshi Yasui1, Yoshihiko Yamamoto1 (1. Grad. Sch. Pharm. Sci., Nagoya Univ.)

[28-61-pm2-35S]Development of Visible-Light-Induced Intramolecular [2+2] Cyclization Using Copper Acetylide Catalysts

○Takayuki Nagano1, Yuiko Sakata1, Keisuke Hikida1, Fuyuhiko Inagaki1,2, Ryo Murakami1,2 (1. Fac. Pharm. Sci.,kobegakuin Univ., 2. Grad. Sch. Pharm. Sci., kobegakuin Univ.)