Iio K - Search Results

1

Enantioselective total synthesis of a potent antitumor antibiotic, fredericamycin A.

Kita Y, Higuchi K, Yoshida Y, Iio K, Kitagaki S, Ueda K, Akai S, Fujioka H. Kita Y, et al. Among authors: iio k. J Am Chem Soc. 2001 Apr 11;123(14):3214-22. doi: 10.1021/ja0035699. J Am Chem Soc. 2001. PMID: 11457055

2

Asymmetric total synthesis of fredericamycin A: an intramolecular cycloaddition pathway.

Akai S, Tsujino T, Fukuda N, Iio K, Takeda Y, Kawaguchi K, Naka T, Higuchi K, Akiyama E, Fujioka H, Kita Y. Akai S, et al. Among authors: iio k. Chemistry. 2005 Oct 21;11(21):6286-97. doi: 10.1002/chem.200500443. Chemistry. 2005. PMID: 16075440

3

Asymmetric Total Synthesis of Fredericamycin A.

Kita Y, Higuchi K, Yoshida Y, Iio K, Kitagaki S, Akai S, Fujioka H. Kita Y, et al. Among authors: iio k. Angew Chem Int Ed Engl. 1999 Mar 1;38(5):683-686. doi: 10.1002/(SICI)1521-3773(19990301)38:5<683::AID-ANIE683>3.0.CO;2-0. Angew Chem Int Ed Engl. 1999. PMID: 29711553

4

Total synthesis of the antitumor antibiotic (+/-)-fredericamycin A by a linear approach.

Kita Y, Iio K, Kawaguchi K, Fukuda N, Takeda Y, Ueno H, Okunaka R, Higuchi K, Tsujino T, Fujioka H, Akai S. Kita Y, et al. Among authors: iio k. Chemistry. 2000 Nov 3;6(21):3897-905. doi: 10.1002/1521-3765(20001103)6:21<3897::aid-chem3897>3.0.co;2-1. Chemistry. 2000. PMID: 11126950

5

Enantiodivergent synthesis of either enantiomer of ABCDE-ring analogue of antitumor antibiotic fredericamycin A via intramolecular [4 + 2] cycloaddition approach.

Akai S, Tsujino T, Fukuda N, Iio K, Takeda Y, Kawaguchi Ki K, Naka T, Higuchi K, Kita Y. Akai S, et al. Among authors: iio k. Org Lett. 2001 Dec 13;3(25):4015-8. doi: 10.1021/ol016696y. Org Lett. 2001. PMID: 11735573

6

An efficient synthesis of peri-hydroxy aromatic compounds via a strong-base-induced.

Iio K, Ramesh NG, Okajima A, Higuchi K, Fujioka H, Akai S, Kita Y. Iio K, et al. J Org Chem. 2000 Jan 14;65(1):89-95. doi: 10.1021/jo990649q. J Org Chem. 2000. PMID: 10813900

7

Ambident effect of a p-sulfinyl group for the introduction of two carbon substituents to phenol rings: a convergent synthesis of diverse benzofuran neolignans.

Akai S, Morita N, Iio K, Nakamura Y, Kita Y. Akai S, et al. Among authors: iio k. Org Lett. 2000 Jul 27;2(15):2279-82. doi: 10.1021/ol0001261. Org Lett. 2000. PMID: 10930263

8

Small-molecule inhibitors of linear ubiquitin chain assembly complex (LUBAC), HOIPINs, suppress NF-κB signaling.

Katsuya K, Oikawa D, Iio K, Obika S, Hori Y, Urashima T, Ayukawa K, Tokunaga F. Katsuya K, et al. Among authors: iio k. Biochem Biophys Res Commun. 2019 Feb 12;509(3):700-706. doi: 10.1016/j.bbrc.2018.12.164. Epub 2019 Jan 2. Biochem Biophys Res Commun. 2019. PMID: 30611571

9

Molecular bases for HOIPINs-mediated inhibition of LUBAC and innate immune responses.

Oikawa D, Sato Y, Ohtake F, Komakura K, Hanada K, Sugawara K, Terawaki S, Mizukami Y, Phuong HT, Iio K, Obika S, Fukushi M, Irie T, Tsuruta D, Sakamoto S, Tanaka K, Saeki Y, Fukai S, Tokunaga F. Oikawa D, et al. Among authors: iio k. Commun Biol. 2020 Apr 3;3(1):163. doi: 10.1038/s42003-020-0882-8. Commun Biol. 2020. PMID: 32246052 Free PMC article.

10

Combined use of alpha-difluoromethylornithine and an inhibitor of S-adenosylmethionine decarboxylase in mice bearing P388 leukemia or Lewis lung carcinoma.

Nakaike S, Kashiwagi K, Terao K, Iio K, Igarashi K. Nakaike S, et al. Among authors: iio k. Jpn J Cancer Res. 1988 Apr;79(4):501-8. doi: 10.1111/j.1349-7006.1988.tb01619.x. Jpn J Cancer Res. 1988. PMID: 3133338 Free PMC article.

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