{"id":427,"date":"2012-05-30T11:00:38","date_gmt":"2012-05-30T02:00:38","guid":{"rendered":"http:\/\/p.bunri-u.ac.jp\/english\/?p=427"},"modified":"2022-04-18T15:49:01","modified_gmt":"2022-04-18T06:49:01","slug":"center-for-instrumental-analysis","status":"publish","type":"post","link":"https:\/\/p.bunri-u.ac.jp\/english\/427\/","title":{"rendered":"Center for Instrumental Analysis"},"content":{"rendered":"

Staff<\/span>
\nProf. Dr. Yoshiyuki Tanaka
\nDr.\u00a0Katsuyuki Nakashima
\nDr. Yasuko Okamoto<\/h2>\n

Publications<\/span><\/p>\n

Original articles<\/strong><\/p>\n

    \n
  1. I. Elshamy, T. Yoneyama, V. T. Nguyem, N. T. Son, Y. Okamoto<\/u>, S. Ban, M. Noji, A. Umeyama, A new cerebroside from the entomopathogenic fungus Ophiocordyceps longiissima: Structual-electronic and antioxidant relationa. Experimental and DFT calculated studies. Jpurnal of molecular Structure, 2020<\/strong>, 1200, 127061.<\/li>\n
  2. Hasegawa, S. Takenaka, M. Oda, H. Domon, T. Hiyoshi, K. Sasagawa, T. Ohsumi, N. Hayashi, Y. Okamoto<\/u>, H. Yamamoto, H. Ohshima, Y. Terao, Y. Noiri, Sulfated vizantin causes detachment of biofilms composed mainly of the genus Streptococcus without affecting bacterial groeth and viability, BMC microbiology, 2020<\/strong>, 20(1), 361.<\/li>\n
  3. Saito, S. Iga, K. Hoshiyama, K. Nakashima<\/u>, Y. Okamoto<\/u>, C. Kuroda, G. Xon, M. Tori. Eremophilane, bakkane, secoeremophilane, and secobakkane sesquiterpenoids from Ligularia virgaurea collected in China.Tetrahedron, 2019<\/strong>, 75, 2239-2245.<\/li>\n
  4. Wada, N. Saito-Tarashima, M. Yamada, Y. Okamoto<\/u>, N. Minagawa. Synthesis of nucleoside units possessing photoreactive diazirine groups on the major and minor groove faces.Tetrahedron Letters, 2019<\/strong>, 60, 1530-1533.<\/li>\n
  5. Saito, Y. Shiosaki, M. Fujiwara, K.Mihara, H. Nakamizo, K. Otose, Y. Okamoto<\/u>, K. Nakashima<\/u>, T. Hanai, C. Kuroda, X. Gong, Y. Matsuo, T. Tanaka, M. Tori. Eremopilanes from Ligularianhookeri collected in China and structural revision of 3\u03b2-Acyloxyfuranoeremophilan-15, 6-olide. Chemical and Pharmaceutical Bulletin<\/em>, 66(6), 2018<\/strong>, 668-673.<\/li>\n
  6. Nakashima<\/u>, K. Hoshiyama, C. Hayama, M. Sakaoku, Y. Okamoto<\/u>, C. Kuroda, X. Gong, M. Tori. Eremophilane sesquiterpenoids and Nor- and Dinoresequiterpenoids from Ligularia virgaurea<\/em> coleected in China. Natural Product Communications<\/em>, 13(7), 2018<\/strong>, 795-798.<\/li>\n
  7. Nishimura, T. Jybo, Y. Okamoto<\/u>, H. Cho. Convergent synthesis of 4,6-unsubstituted 5-acyl-aminohydropyrimidines using Weinreb amide. Terahedron Letters<\/em>, 58, 2017<\/strong>, 4236-4239.<\/li>\n
  8. Saito, M. Hidaka, A. Fukuda, Y. Okamoto<\/u>, K. Nakashima<\/u>, M. Tori, R. Hanai, X. Gong, E. Watanabe, C. Kuroda. Intra-specific diversity of the chemical composition of Ligularia lamarum<\/em> in the Hengduan Mountains, China: The structures of four new eremophilanes and a new seco-eremophilane. Phytochemistry Letters<\/em>, Volume 20, 2017<\/strong>, Pages 139-145.<\/li>\n
  9. Okamoto<\/u>, M. Taniguchi, K. Nakashima<\/u>, X. Gong, R. Hanai, C. Kuroda, M. Tori. Chemical Constituents of Ligularia wilsoniana<\/em> Collected in Chongqing, China. Natural product communications<\/em>, 11<\/strong> (2), 2016<\/strong>, 149-152.<\/li>\n
  10. Okamoto<\/u>, M. Taniguchi, K. Terada, K. Nakashima<\/u>, X. Gong, R. Hanai, M. Tori, C. Kuroda. Diversity in Chemical Constituents of Ligularia longihastata<\/em> Collected in China. Natural product communications<\/em>, 11<\/strong> (2), 2016<\/strong>, 145-148.<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"

    Staff Prof. Dr. Yoshiyuki Tanaka Dr.\u00a0Katsuyuki Nakashima Dr. Yasuko Okamoto Publications Original articles I. … \u7d9a\u304d\u3092\u8aad\u3080 Center for Instrumental Analysis<\/span><\/a><\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[37],"tags":[],"_links":{"self":[{"href":"https:\/\/p.bunri-u.ac.jp\/english\/wp-json\/wp\/v2\/posts\/427"}],"collection":[{"href":"https:\/\/p.bunri-u.ac.jp\/english\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/p.bunri-u.ac.jp\/english\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/p.bunri-u.ac.jp\/english\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/p.bunri-u.ac.jp\/english\/wp-json\/wp\/v2\/comments?post=427"}],"version-history":[{"count":11,"href":"https:\/\/p.bunri-u.ac.jp\/english\/wp-json\/wp\/v2\/posts\/427\/revisions"}],"predecessor-version":[{"id":950,"href":"https:\/\/p.bunri-u.ac.jp\/english\/wp-json\/wp\/v2\/posts\/427\/revisions\/950"}],"wp:attachment":[{"href":"https:\/\/p.bunri-u.ac.jp\/english\/wp-json\/wp\/v2\/media?parent=427"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/p.bunri-u.ac.jp\/english\/wp-json\/wp\/v2\/categories?post=427"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/p.bunri-u.ac.jp\/english\/wp-json\/wp\/v2\/tags?post=427"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}