M
Masaru Kondo
Researcher at Osaka University
Publications - 6
Citations - 72
Masaru Kondo is an academic researcher from Osaka University. The author has contributed to research in topics: Catalysis & Denticity. The author has an hindex of 3, co-authored 6 publications receiving 19 citations. Previous affiliations of Masaru Kondo include Ibaraki University.
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Journal ArticleDOI
Photoswitchable Chiral Phase Transfer Catalyst
TL;DR: Azo-crown ether-based photoswitching chiral phase transfer catalysts have been developed to control the catalytic activity by photoirradiation as mentioned in this paper, which can switch i.e.
Journal ArticleDOI
Exploration of flow reaction conditions using machine-learning for enantioselective organocatalyzed Rauhut–Currier and [3+2] annulation sequence
Masaru Kondo,H. D. P. Wathsala,Makoto Sako,Yutaro Hanatani,Kazunori Ishikawa,Satoshi Hara,Takayuki Takaai,Takashi Washio,Shinobu Takizawa,Hiroaki Sasai +9 more
TL;DR: A highly atom-economical enantioselective organocatalyzed Rauhut-Currier and [3+2] annulation sequence has been established by using a flow system and functionalized chiral spirooxindole analogues were obtained in high yield.
Journal ArticleDOI
Energy-, time-, and labor-saving synthesis of α-ketiminophosphonates: machine-learning-assisted simultaneous multiparameter screening for electrochemical oxidation
Masaru Kondo,Masaru Kondo,Akimasa Sugizaki,Md. Imrul Khalid,H. D. P. Wathsala,Kazunori Ishikawa,Satoshi Hara,Takayuki Takaai,Takashi Washio,Shinobu Takizawa,Hiroaki Sasai +10 more
TL;DR: In this paper, a highly efficient synthesis of α-ketiminophosphonates has been established for the electrochemical oxidation of αamino phosphonates with the utilization of machine-learning-assisted simultaneous multiparameter screening.
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Room-Temperature, Metal-Free, and One-Pot Preparation of 2H-Indazoles through a Mills Reaction and Cyclization Sequence.
TL;DR: The Mills reaction and cyclization of readily available 2-aminobenzyl alcohols and nitrosobenzenes using thionyl bromide provided 2H-indazoles in up to 88 % yields and in the metal-free process, acetic acid played a crucial role for the both Mills Reaction and Cyclization.
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Azopyridine-based chiral oxazolines with rare-earth metals for photoswitchable catalysis.
TL;DR: In this article, an azopyridine-based oxazoline was developed for utilizing azo group coordination and isomerization as a photoswitchable ligand, which enabled modulation of the enantioselectivity of an rare-earth metal (RE) catalyzed aminal forming reaction.