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Year | Number of Results |
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2010 | 3 |
2011 | 1 |
2012 | 1 |
2013 | 2 |
2024 | 0 |
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Page 1
Metal-free C-H cross-coupling toward oxygenated naphthalene-benzene linked biaryls.
Org Lett. 2011 Dec 2;13(23):6208-11. doi: 10.1021/ol202632h. Epub 2011 Oct 28.
Org Lett. 2011.
PMID: 22035315
Unusual ipso substitution of diaryliodonium bromides initiated by a single-electron-transfer oxidizing process.
Dohi T, Ito M, Yamaoka N, Morimoto K, Fujioka H, Kita Y.
Dohi T, et al. Among authors: yamaoka n.
Angew Chem Int Ed Engl. 2010 Apr 26;49(19):3334-7. doi: 10.1002/anie.200907281.
Angew Chem Int Ed Engl. 2010.
PMID: 20405520
No abstract available.
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Enhanced reactivity of [hydroxy(tosyloxy)iodo]benzene in fluoroalcohol media. Efficient direct synthesis of thienyl(aryl)iodonium salts.
Ito M, Ogawa C, Yamaoka N, Fujioka H, Dohi T, Kita Y.
Ito M, et al. Among authors: yamaoka n.
Molecules. 2010 Mar 17;15(3):1918-31. doi: 10.3390/molecules15031918.
Molecules. 2010.
PMID: 20336022
Free PMC article.
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Single-electron-transfer (SET)-induced oxidative biaryl coupling by polyalkoxybenzene-derived diaryliodonium(III) salts.
Yamaoka N, Sumida K, Itani I, Kubo H, Ohnishi Y, Sekiguchi S, Dohi T, Kita Y.
Yamaoka N, et al.
Chemistry. 2013 Oct 25;19(44):15004-11. doi: 10.1002/chem.201301148. Epub 2013 Sep 17.
Chemistry. 2013.
PMID: 24105695
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Efficient synthesis of a regioregular oligothiophene photovoltaic dye molecule, MK-2, and related compounds: a cooperative hypervalent iodine and metal-catalyzed synthetic route.
Dohi T, Yamaoka N, Nakamura S, Sumida K, Morimoto K, Kita Y.
Dohi T, et al. Among authors: yamaoka n.
Chemistry. 2013 Feb 4;19(6):2067-75. doi: 10.1002/chem.201203503. Epub 2012 Dec 23.
Chemistry. 2013.
PMID: 23280683
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Metal-free regioselective oxidative biaryl coupling leading to head-to-tail bithiophenes: reactivity switching, a concept based on the iodonium(III) intermediate.
Morimoto K, Yamaoka N, Ogawa C, Nakae T, Fujioka H, Dohi T, Kita Y.
Morimoto K, et al. Among authors: yamaoka n.
Org Lett. 2010 Sep 3;12(17):3804-7. doi: 10.1021/ol101498r.
Org Lett. 2010.
PMID: 20690618
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