Akitoshi Fujiya
Gifu Pharmaceutical University
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Publication
Featured researches published by Akitoshi Fujiya.
Organic Letters | 2013
Tomoya Nobuta; Norihiro Tada; Akitoshi Fujiya; Atsumasa Kariya; Tsuyoshi Miura; Akichika Itoh
A useful method for molecular iodine catalyzed oxidative C-C bond formation between tertiary amines and a carbon nucleophile using hydrogen peroxide as the terminal oxidant is reported. This is the first report of a molecular iodine catalyzed cross-dehydrogenative coupling (CDC) reaction between two sp(3) C-H bonds.
Journal of Organic Chemistry | 2016
Akitoshi Fujiya; Masanori Tanaka; Eiji Yamaguchi; Norihiro Tada; Akichika Itoh
We report an efficient method for the synthesis of pyrrolo[2,1-a]isoquinoline derivatives using sequential [3 + 2] cycloaddition/oxidative aromatization reactions catalyzed by methylene blue with fluorescent light irradiation under an oxygen atmosphere. The products were obtained in moderate to good yields.
RSC Advances | 2013
Tomoya Nobuta; Akitoshi Fujiya; Tomoaki Yamaguchi; Norihiro Tada; Tsuyoshi Miura; Akichika Itoh
This paper reports a useful method for molecular-iodine-catalyzed aerobic photooxidative C–C bond formation between tertiary amines and carbon nucleophiles. This reaction provides a practical method for C–C bond formation through the use of molecular iodine, harmless visible light irradiation, and molecular oxygen as the terminal oxidant.
RSC Advances | 2015
Akitoshi Fujiya; Tomoya Nobuta; Eiji Yamaguchi; Norihiro Tada; Tsuyoshi Miura; Akichika Itoh
We report an aerobic photooxidative direct asymmetric aldol reaction using water as the solvent. In this reaction, primary benzyl alcohols are oxidized into benzaldehydes under an oxygen atmosphere using anthraquinone-2-sodium sulfonate monohydrate as an organophotocatalyst. Stereoselective aldol reactions then proceed using a proline-type organocatalyst.
RSC Advances | 2018
Masato Deguchi; Akitoshi Fujiya; Eiji Yamaguchi; Norihiro Tada; Bunji Uno; Akichika Itoh
Herein, we reported an attractive method for synthesizing medium-sized rings that are catalyzed by erythrosine B under fluorescent light irradiation. This synthetic approach featured mild conditions, a facile procedure, a broad substrate scope, and moderate-to-good yields.
Synlett | 2012
Tomoya Nobuta; Akitoshi Fujiya; Norihiro Tada; Tsuyoshi Miura; Akichika Itoh
Tetrahedron Letters | 2014
Izuho Itoh; Yoko Matsusaki; Akitoshi Fujiya; Norihiro Tada; Tsuyoshi Miura; Akichika Itoh
Tetrahedron Letters | 2012
Tomoya Nobuta; Akitoshi Fujiya; Shin-ichi Hirashima; Norihiro Tada; Tsuyoshi Miura; Akichika Itoh
Synlett | 2014
Akitoshi Fujiya; Atsumasa Kariya; Tomoya Nobuta; Norihiro Tada; Tsuyoshi Miura; Akichika Itoh
Synlett | 2015
Akifumi Okada; Hiroki Yuasa; Akitoshi Fujiya; Norihiro Tada; Tsuyoshi Miura; Akichika Itoh