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Tetrahedron Letters|December 4, 2008
Effective Procedure for Selective Ammonolysis of Monosubstituted Oxiranes: Application to E7389 SynthesisYosuke Kaburagi, Yoshito KishiOrganic Letters|February 9, 2007
Operationally simple and efficient workup procedure for TBAF-mediated desilylation: application to halichondrin synthesisYosuke Kaburagi, Yoshito KishiJournal of the American Chemical Society|August 19, 2004
Total synthesis of (-)-strychnineYosuke Kaburagi, Hidetoshi Tokuyama, Tohru FukuyamaJournal of the American Chemical Society|April 3, 2003
Total synthesis of leustroducsin BKousei Shimada, Yosuke Kaburagi, Tohru FukuyamaChemical Biology & Drug Design|November 5, 2022
Identification of a novel ALDH1A3-selective inhibitor by a chemical probe with unrelated bioactivity: An approach to affinity-based drug target discoveryHiroshi Kamiyama, Masayuki Miyano, Daisuke Ito, et al.Journal of the American Chemical Society|October 8, 2009
New syntheses of E7389 C14-C35 and halichondrin C14-C38 building blocks: reductive cyclization and oxy-Michael cyclization approachesCheng-Guo Dong, James A Henderson, Yosuke Kaburagi, et al.Scientific Reports|June 19, 2019
A landmark in drug discovery based on complex natural product synthesisSatoshi Kawano, Ken Ito, Kenzo Yahata, et al.Organic Letters|January 22, 2024
Ten-Gram-Scale Total Synthesis of the Anticancer Drug Candidate E7130 to Supply Clinical TrialsYosuke Kaburagi, Kazunobu Kira, Kenzo Yahata, et al.Pageof 1