Session Details

[29-09-am]Chemical reaction development, mechanistic analysis, computational chemistry 11

Sat. Mar 29, 2025 8:30 AM - 10:11 AM JST
Sat. Mar 29, 2025 11:30 PM - 1:11 AM UTC
Room 9 (Fukuoka International Congress Center: 411 [4F])
Chair: Shinichiro Fuse, Masahiro Egi

[29-09-am01]Development of continuous flow hydrogenation and reductive alkylation using etched silicon powder-supported palladium as a durable catalyst

○Zhenzhong Zhang1, Heeyoel Baek1, Eman Soliman1,2, Yoichi M. A. Yamada1,2 (1. RIKEN CSRS, 2. Grad. Sch. Sci. Eng., Saitama Univ.)

[29-09-am02S]Monoacylation of diols enabled by resin catalysis

Yusuke Kuroda1,2, ○Keigo Sonokawa1, Kiyosei Takasu1 (1. Grad. Sch. Pharm. Sci., Kyoto Univ., 2. The Hakubi Center for Advanced Research)

[29-09-am03S]Development of electrochemically assisted deprotection method for cyclic acetals without the addition of water

○Yuka Abe1, Takashi Ikawa1, Hironao Sajiki1, Tsuyoshi Yamada2 (1. Gifu. Pharm. Univ., 2. Faculty of Pharm. Sci., University of Toyama)

[29-09-am04S]Catalytic Reductive Amination Using Carboxylic Acids as Substrates

○Kento Nakamura1, Ryosuke Tsutsumi1, Naoya Kumagai1,2 (1. Graduate School of Pharmaceutical Sciences, Keio University, 2. Institute of Microbial Chemistry)

Break

[29-09-am05]Reductive N-alkylation of amides using CuBr2 and 1,1,3,3-tetramethyldisiloxane

○Tomoya Nobuta1, Noriyuki Yamagiwa1, Yutaka Suto1 (1. Faculty of Pharmacy, Takasaki Univ. of Health and Welfare)

[29-09-am06]Conversion of Amides into Esters Using Sulfonium Salt

○sho inagaki1, kazuto kobayashi1, ryuhi yamaguchi1, tatsuya natsui1, tomikazu kawano1 (1. Iwate Medical University, School of Pharmacy)

[29-09-am07S]α-Selective C–H alkylation of α-silyl alcohols using phosphonium ylides as hydrogen atom transfer catalysts

○Yuto Arai1, Shunsuke Ogura1, Akira Matsumoto1, Chao Wang1, Keiichi Hirano1 (1. Faculty of Pharmaceutical Sciences, Institute of Medical, Pharmaceutical, and Health Sciences, Kanazawa University)

[29-09-am08S]Carboxy group selective modification using oxymoyl halides under aqueous conditions.

○Kaho Hyakunari1, Koki Imai1, Kenji Mishiro1,2 (1. Grad. Sch. Pharm., Kanazawa Univ., 2. InFiniti., Kanazawa Univ.)