Session Details
[29-61-pm1]Chemical reaction development, mechanistic analysis, computational chemistry 15
Sun. Mar 29, 2026 1:10 PM - 3:10 PM JST
Sun. Mar 29, 2026 4:10 AM - 6:10 AM UTC
Sun. Mar 29, 2026 4:10 AM - 6:10 AM UTC
Room 61 (4201, Bldg. 4, Area 4 [2F]) (4)
Discusser: Masahiro Abe, Yasukawa Naoki
[29-61-pm1-33]Diversity-Oriented Synthesis of Phosphacyclic compounds
○Takehiro Yamagishi1, Araki Kutanida1, Atsuki Goto1, Shino Nakajima1, Shintaro Kamio1 (1. Dept. of Medicinal Chemistry, Faculty of Pharm. Sci., Hokkaido Univ. of Sci.)
[29-61-pm1-34S]Construction of a Dihydroquinolinone Framework via Consecutive Ring-Opening/Cyclization of Alkynylazetidinones.
○TOYA KARIYA1, Masahiro Yoshida1 (1. Faculty of Pharmaceutical Sciences, Tokushima Bunri University)
[29-61-pm1-35S]β-Selective C–H Alkylation of Phosphonium Ylidesvia Cooperative Photoredox-Brønsted Base Catalysis
○Shunsuke Ogura1, Akira Matsumoto2, Chao Wang2, Keiichi Hirano2,3 (1. Sch.Pharm., Kanazawa Univ., 2. Grad. Sch. Pharm. Sci., Kanazawa Univ., 3. JST)
[29-61-pm1-36]DMAPO/Boc2O-Mediated One-Pot Direct N-Acylation of Sulfoximines and Oxazolidinones with Carboxylic Acids
○atsushi umehara1, Sukenao Kawai1, Makoto Sasaki1 (1. Grad. Sch. Life Sci., Tohoku Univ.)
[29-61-pm1-37]Synthesis of 1-aryl-4-arylselanyl-1H-pyrazoles: Silver-catalyzed three-component reaction of 1H-pyrazoles, arylboronic acids, and selenium
○Yuki Murata1, Kousuke Tajima1, Yasuhiro Nagai1, Mio Matsumura1, Shuji Yasuike1 (1. Sch. Pharm. Sci., Aichigakuin Univ.)
[29-61-pm1-38S]Au vs Ag Catalysis: Metal-Controlled Chemodivergent Reactivity of Cyclic α-Hydroxy Iminium Ion
○Yuto Yoshikawa1, Tomoya Wakana1, Kohei Watanabe2, Haraguchi Ryosuke1 (1. Grad. Sch. Eng., Chiba Inst. Tech., 2. Fac. Educ., Chiba Univ.)
[29-61-pm1-39S]Gold-Catalyzed Consecutive Ring-Opening/Cyclization of Alkynylcyclopropanes with Heteroatom-Containing Nucleophiles.
○Kyota Okada1, Aoi Kimura1, Shinya Shiomi1, Masahiro Yoshida1 (1. Faculty of Pharmaceutical Sciences, Tokushima Bunri University)
[29-61-pm1-40S]Aza-Hosomi-Sakurai reaction by B(OH)3/biphenol catalyst system
○Ami Kato1, Kenji Sugimoto1 (1. Grad. Sch. Life and Environmental Sci., Kyoto Pref Univ.)
[29-61-pm1-41S]Synthetic Study of Renieramycins Construction of the Characteristic CDE-ring Model
○Hiroto Tsukui1, Tatsuki Yamada1, Ryo Sato1, Shinya Kimura1, Naoki Saito1, Masashi Yokoya1 (1. Meiji Pharm. Univ.)
[29-61-pm1-42S]Development of a Synthetic Method for Acid Fluorides with Broad Functional-Group Tolerance
○Akari Yoshizaki1, Ayumi Tokumasu1, Eiko Kujime1, Ryosuke Saijo1, Masanori Kitamura1 (1. Fac. Pharm. Sci., Matsuyama Univ.)
[29-61-pm1-43S]Synthesis of 3,3-disubsituted succinimides bearing all-carbon quaternary centers and stereoselective construction of the indolizino[8,7-b]indole skeleton
○Fuka Nakabayashi1, Masafumi Tamura1 (1. Department of Pharmacy, Sanyo-Onoda City Univ.)
