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A mild conversion from 3-vinyl- to 3-formyl-chlorophyll derivatives
A mild conversion from 3-vinyl- to 3-formyl-chlorophyll derivatives
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A mild conversion from 3-vinyl- to 3-formyl-chlorophyll derivatives

Oba, Toru ; Uda, Yuki ; Matsuda, Kohei ; Fukusumi, Takanori ; Ito, Satoshi ; Hiratani, Kazuhisa ; Tamiaki, Hitoshi

Bioorganic & medicinal chemistry letters, 2011-04, Vol.21 (8), p.2489-2491 [Periódico revisado por pares]

Amsterdam: Elsevier Ltd

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2
Non-enzymatic conversion of chlorophyll-a into chlorophyll-d in vitro: A model oxidation pathway for chlorophyll-d biosynthesis
Non-enzymatic conversion of chlorophyll-a into chlorophyll-d in vitro: A model oxidation pathway for chlorophyll-d biosynthesis
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Non-enzymatic conversion of chlorophyll-a into chlorophyll-d in vitro: A model oxidation pathway for chlorophyll-d biosynthesis

Fukusumi, Takanori ; Matsuda, Kohei ; Mizoguchi, Tadashi ; Miyatake, Tomohiro ; Ito, Satoshi ; Ikeda, Tsukasa ; Tamiaki, Hitoshi ; Oba, Toru

FEBS letters, 2012-07, Vol.586 (16), p.2338-2341 [Periódico revisado por pares]

England: Elsevier B.V

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3
Alternative synthesis of 3-acetyl, 3-epoxy, and 3-formyl chlorins from a 3-vinyl chlorin, methyl pyropheophorbide-a, via iodination
Alternative synthesis of 3-acetyl, 3-epoxy, and 3-formyl chlorins from a 3-vinyl chlorin, methyl pyropheophorbide-a, via iodination
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Alternative synthesis of 3-acetyl, 3-epoxy, and 3-formyl chlorins from a 3-vinyl chlorin, methyl pyropheophorbide-a, via iodination

Oba, Toru ; Masuya, Takuto ; Yasuda, Satoru ; Ito, Satoshi

Bioorganic & medicinal chemistry letters, 2015-08, Vol.25 (15), p.3009-3012 [Periódico revisado por pares]

England: Elsevier Ltd

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4
Facile iodination of the vinyl groups in protoporphyrin IX dimethyl ester and subsequent transformation of the iodinated moieties
Facile iodination of the vinyl groups in protoporphyrin IX dimethyl ester and subsequent transformation of the iodinated moieties
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Facile iodination of the vinyl groups in protoporphyrin IX dimethyl ester and subsequent transformation of the iodinated moieties

Miyata, Kota ; Yasuda, Satoru ; Masuya, Takuto ; Ito, Satoshi ; Kinoshita, Yusuke ; Tamiaki, Hitoshi ; Oba, Toru

Tetrahedron, 2018-07, Vol.74 (27), p.3707-3711 [Periódico revisado por pares]

Elsevier Ltd

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5
Selective synthesis of C3 super(2)- and C20-monoiodinated chlorophyll derivatives
Selective synthesis of C3 super(2)- and C20-monoiodinated chlorophyll derivatives
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Selective synthesis of C3 super(2)- and C20-monoiodinated chlorophyll derivatives

Oba, Toru ; Miyata, Kota ; Masuya, Takuto ; Yasuda, Satoru ; Ito, Satoshi

Tetrahedron letters, 2015-02, Vol.56 (8), p.999-1003 [Periódico revisado por pares]

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6
Synthesis and photophysical properties of phenyl-sulfanylated chlororophyll derivatives
Synthesis and photophysical properties of phenyl-sulfanylated chlororophyll derivatives
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Synthesis and photophysical properties of phenyl-sulfanylated chlororophyll derivatives

Takei, Natsuki ; Morioka, Misaki ; Yoshizato, Mari ; Tanaka, Takuya ; Sasaki, Shin-ichi ; Ito, Satoshi ; Tamiaki, Hitoshi ; Oba, Toru

Tetrahedron, 2014-08, Vol.70 (34), p.5109-5113 [Periódico revisado por pares]

Elsevier Ltd

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7
Radical reaction of chlorophyll derivatives triggered by AIBN
Radical reaction of chlorophyll derivatives triggered by AIBN
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Radical reaction of chlorophyll derivatives triggered by AIBN

Oba, Toru ; Tateno, Yubi ; Ihara, Misaki ; Fukusumi, Takanori ; Takei, Natsuki ; Ito, Satoshi

Tetrahedron letters, 2014-01, Vol.55 (3), p.725-727 [Periódico revisado por pares]

Elsevier Ltd

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8
Selective synthesis of C32- and C20-monoiodinated chlorophyll derivatives
Selective synthesis of C32- and C20-monoiodinated chlorophyll derivatives
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Selective synthesis of C32- and C20-monoiodinated chlorophyll derivatives

Oba, Toru ; Miyata, Kota ; Masuya, Takuto ; Yasuda, Satoru ; Ito, Satoshi

Tetrahedron letters, 2015-02, Vol.56 (8), p.999-1003 [Periódico revisado por pares]

Elsevier Ltd

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9
Ene-thiol reaction of C3-vinylated chlorophyll derivatives in the presence of oxygen: synthesis of C3-formyl-chlorins under mild conditions
Ene-thiol reaction of C3-vinylated chlorophyll derivatives in the presence of oxygen: synthesis of C3-formyl-chlorins under mild conditions
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Ene-thiol reaction of C3-vinylated chlorophyll derivatives in the presence of oxygen: synthesis of C3-formyl-chlorins under mild conditions

Fukusumi, Takanori ; Takei, Natsuki ; Tateno, Yubi ; Aoki, Takuya ; Ando, Ai ; Kozakai, Kouhei ; Shima, Hiroko ; Mizoguchi, Tadashi ; Ito, Satoshi ; Ikeda, Tsukasa ; Tamiaki, Hitoshi ; Oba, Toru

Journal of porphyrins and phthalocyanines, 2013-12, Vol.17 (12), p.1188-1195 [Periódico revisado por pares]

Singapore: World Scientific Publishing Company

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