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Journal of Natural Products|December 9, 2022
Krasilnikolides A and B and Detalosylkrasilnikolide A, Cytotoxic 20-Membered Macrolides from the Genus Krasilnikovia: Assignment of Anomeric Configuration by J-Based Configuration AnalysisShiyang Lu, Tao Zhou, Keisuke Fukaya, et al.The Journal of Antibiotics|April 14, 2023
Isolation and structure determination of allopteridic acids A-C and allokutzmicin from an unexplored actinomycete of the genus AllokutzneriaChang Liu, Zhiwei Zhang, Keisuke Fukaya, et al.Organic Letters|November 26, 2025
Total Synthesis of Racemic Benzosceptrins via an Electrocyclization CascadeYudai Fujino, Taisei Matoba, Ayami Amano, et al.The Journal of Antibiotics|September 8, 2022
Cyclic enaminones and a 4-quinazolinone from an unidentified actinomycete of the family MicromonosporaceaeDesy W Triningsih, Tao Zhou, Keisuke Fukaya, et al.Bioscience, Biotechnology, and Biochemistry|October 27, 2025
Synthesis of the decalin structure of cladoic acidAzumi Kasashima, Md Masud Rana, Taisei Matoba, et al.Journal of Biochemistry|January 8, 2013
Stereochemical assignment and anti-inflammatory properties of the omega-3 lipid mediator resolvin E3Yosuke Isobe, Makoto Arita, Ryo Iwamoto, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|August 3, 2005
Total synthesis of murisolins and evaluation of tumor-growth inhibitory activityNaoyoshi Maezaki, Hiroaki Tominaga, Naoto Kojima, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|December 1, 2015
Symmetry-Driven Strategy for the Assembly of the Core Tetracycle of (+)-Ryanodine: Synthetic Utility of a Cobalt-Catalyzed Olefin Oxidation and α-Alkoxy Bridgehead Radical ReactionMasanori Nagatomo, Koji Hagiwara, Kengo Masuda, et al.Molecules (Basel, Switzerland)|June 26, 2012
Asymmetric synthesis of the carbon-14-labeled selective glucocorticoid receptor modulator using cinchona alkaloid catalyzed addition of 6-bromoindole to ethyl trifluoropyruvateTakaaki Sumiyoshi, Daisuke Urabe, Kengo Tojo, et al.The Journal of Organic Chemistry|October 5, 2018
Total Synthesis and Biological Evaluation of 19-Hydroxysarmentogenin-3 -O-α-l-rhamnoside, Trewianin, and Their AglyconsDaisuke Urabe, Yuki Nakagawa, Ken Mukai, et al.Pageof 8