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<title>H27　化学　森山　克彦　</title>
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<p class=MsoNormal align=left style='text-align:left'><b><span lang=EN-US>2015</span></b><b><span
style='font-family:"ＭＳ 明朝","serif"'>年度（平成</span></b><b><span lang=EN-US>27</span></b><b><span
style='font-family:"ＭＳ 明朝","serif"'>年度）</span></b></p>

<p class=MsoNormal align=left style='text-align:left'><span style='font-family:
"ＭＳ 明朝","serif"'>コース名　　化学コース</span></p>

<p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>領域名　　　機能物質化学領域</span></p>

<p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>教員名　　　森山　克彦</span></p>

<p class=MsoNormal style='margin-left:105.0pt;text-indent:-105.0pt'><span
style='font-family:"ＭＳ 明朝","serif"'>電子メール　</span>moriyama
<span style='font-family:"ＭＳ 明朝","serif"'>理 </span><span lang=EN-US>faculty.chiba-u.jp</span></p>

<p class=MsoNormal style='margin-left:105.0pt;text-indent:-105.0pt'><span
style='font-family:"ＭＳ 明朝","serif"'>　　　　　　※メール送信の際は、「理」を半角</span><span
lang=EN-US>@</span><span style='font-family:"ＭＳ 明朝","serif"'>に変更してください。</span></p>

<p class=MsoNormal><b><span lang=EN-US>&nbsp;</span></b></p>

<p class=MsoNormal><b><span style='font-family:"ＭＳ 明朝","serif"'>（</span><span
lang=EN-US>1</span><span style='font-family:"ＭＳ 明朝","serif"'>)研究論文などのリスト(印刷中を含む)</span></b></p>
<p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>　　　</span></p>
<table width="940" border="1">
  <tr>
    <td width="37"></td>
    <td width="117"><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>著者・発表者等</span></p></td>
    <td width="187"><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>タイトル</span></p></td>
    <td width="185"><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>発表雑誌・会合等</span></p></td>
    <td width="60"><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>巻・号</span></p></td>
    <td width="76"><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>頁</span></p></td>
    <td width="32"><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>発行・発表年等</span></p></td>
    <td width="194"><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>掲載論文のDOI(付与されている場合)</span></p></td>
  </tr>
  <tr>
    <td>　(1)</td>
    <td><p class=MsoNormal><span lang=EN-US>Katsuhiko<br>
 Moriyama,<br>
 Kazuma<br>
 Ishida,<br>
 Hideo Togo</span></p>

    </td>
    <td><p class=MsoNormal><span lang=EN-US>Regioselective C<sub>sp2</sub>–H dual<br>
 functionalization of indoles using<br>
 hypervalent iodine(III):<br>
 bromo-amination <i>via</i><br>
 1,3-migration of imides on<br>
 indolyl(phenyl)iodonium imides</span></p></td>  
    
    <td><p class=MsoNormal><span lang=EN-US>Chemical<br>
 Communication</span></p></td>
    <td><p class=MsoNormal>51</p></td>
    <td><p class=MsoNormal><span lang=EN-US>pp.2273-2276</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>2015</span></p></td>
    <td><p class=MsoNormal>10.1039/C4CC09077B</p></td>
  </tr>
  <tr>
    <td>　(2)</td>
    <td><p class=MsoNormal><span lang=EN-US>Toshiyuki<br>
 Tamura,<br>
 Katsuhiko<br>
 Moriyama,<br>
 Hideo Togo</span></td>
    <td><p class=MsoNormal><span lang=EN-US>Facile One-Pot Transformation of<br>
 Arenes into Aromatic Nitriles<br>
 under Metal-Cyanide-Free<br>
 Conditions</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>European<br>
 Journal of<br>
 Organic<br>
 Chemistry</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>2015　</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>pp.2023-2029</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>2015</span></p></td>
    <td><p class=MsoNormal>10.1002/ejoc.201403672</p></td>
  </tr>
    <tr>

    <td>　(3)</td>
    <td><p class=MsoNormal><span lang=EN-US>Hiroyuki<br>
 Shimojo,<br>
 Katsuhiko<br>
 Moriyama,<br>
 Hideo Togo<br></span></p>
    </td>

    <td><p class=MsoNormal><span lang=EN-US>A One-Pot,<br>
 Transition-Metal-Free Procedure<br>
 for C–O, C–S, and C–N Bond<br>
 Formation at the Benzylic<br>
 Position of Methylarenes</span></p></td>      

    <td><p class=MsoNormal><span lang=EN-US>Synthesis</span></p></td>

    <td><p class=MsoNormal>47</p></td>
    <td><p class=MsoNormal><span lang=EN-US>p. 1280-1290</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>2015</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>10.1055/s-0034-1380069</span></p></td>
  </tr>

  <tr>
    <td>　(4)</td>
    <td><p class=MsoNormal><span lang=EN-US>Katsuhiko<br>
 Moriyama,<br>
 Toru<br>
 Sugiue,<br>
 Yuki Saito,<br>
 Shoichi<br>
 Katsuta,<br>
 Hideo Togo</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>2,6-Bis(amido)benzoic Acid with<br>
 Internal Hydrogen Bond as<br>
 Brønsted Acid Catalyst for<br>
 Friedel–Crafts Reaction of<br>
 Indoles</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>Advanced<br>
 Synthesis &<br>
 Catalysis</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>357</span></p></td>
    <td><p class=MsoNormal>pp.2143-2149</p></td>
    <td><p class=MsoNormal><span lang=EN-US>2015</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>10.1002/adsc.201401189</span></p></td>
  </tr>

    <tr>
    <td>　(5)</td>
    <td><p class=MsoNormal><span lang=EN-US>Sho Imai,<br>
 Hiroki<br>
 Kikui,<br>
 Katsuhiko<br>
 Moriyama,<br>
 Hideo Togo</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>One-pot preparation of<br>
 2,5-disubstituted and<br>
 2,4,5-trisubstituted oxazoles from<br>
 aromatic ketones with molecular<br>
 iodine, oxone, and<br>
 trifluoromethanesulfonic acid in<br>
 nitriles</span></p></td>  
    
    <td><p class=MsoNormal><span lang=EN-US>Tetrahedron</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>71</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>pp.5267-5274</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>2015</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>10.1016/j.tet.2015.06.022</span></p></td>
  </tr>

  <tr>
    <td>　(6)</td>
    <td><p class=MsoNormal><span lang=EN-US>Naoki<br>
 Okugawa,<br>
 Katsuhiko<br>
 Moriyama,<br>
 Hideo Togo</span></p>  
    </td>

    <td><p class=MsoNormal><span lang=EN-US>Introduction of Ether Groups<br>
 onto Electron-Deficient<br>
 Nitrogen-Containing<br>
 Heteroaromatics Using Radical<br>
 Chemistry under<br>
 Transition-Metal-Free Conditions</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>European<br>
 Journal of<br>
 Organic<br>
 Chemistry</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>2015</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>pp.4793-4981</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>2015</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>10.1002/ejoc.201500584</span></p></td>

    <tr></tr>

    <td>　(7)</td>
    <td><p class=MsoNormal><span lang=EN-US>Katsuhiko<br>
 Moriyama,<br>
 Toru<br>
 Sugiue,<br>
 Chihiro<br>
 Nishinohara,<br>
 Hideo Togo</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>Divergent Synthesis of<br>
 &alpha; ,&gamma; -Disubstituted<br>
 &gamma; -Butyrolactones through<br>
 Diastereoselective<br>
 Bromo-lactonization Using<br>
 Alkali Metal Bromides</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>The Journal of<br>
 Organic<br>
 Chemistry</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>80</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>p.9132-9140</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>2015</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>10.1021/acs.joc.5b01497</span></p></td>

  <tr>
    <td>　(8)</td>
    <td><p class=MsoNormal><span lang=EN-US>Katsuhiko<br>
 Moriyama,<br>
 Chihiro<br>
 Nishinohara,<br>
 Toru<br>
 Sugiue,<br>
 Hideo Togo</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>Oxidative Oxygen-Nucleophilic<br>
 Bromo-Cyclization of Alkenyl<br>
 Carbonyl Compounds Without<br>
 Organic Wastes Using Alkali<br>
 Metal Reagents in Green Solvent</span></p></td>

    <td><p class=MsoNormal><span lang=EN-US>RSC Advances</span></p></td>

    <td><p class=MsoNormal>5</p></td>
    <td><p class=MsoNormal><span lang=EN-US>pp.85872-85878</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>2015</span></p></td>
    <td><p class=MsoNormal>10.1039/C5RA19851H</p></td>
  </tr>

    <tr>
    <td>　(9)</td>
    <td><p class=MsoNormal><span lang=EN-US>Masatoshi<br>
 Ezawa,<br>
 Katsuhiko<br>
 Moriyama,<br>
 Hideo Togo</span></p></td>      

    <td><p class=MsoNormal><span lang=EN-US>Transformation of<br>
 <i>N,N</i>-diisopropylarylmethylamines<br>
 into<br>
 <i>N</i.-isopropylarylmethylamines<br>
 with molecular iodine</span></p></td>

   <td><p class=MsoNormal><span lang=EN-US>Tetrahedron<br>
 Letters</span></p></td>

     <td><p class=MsoNormal>56</p></td>
        <td><p class=MsoNormal><span lang=EN-US>pp.6689-6692</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>2015</span></p></td>
    <td><p class=MsoNormal><span lang=EN-US>10.1016/j.tetlet.2015.10.044</span></p></td>
  </tr>
 </table>

<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>

<p class=MsoNormal><b><span style='font-family:"ＭＳ 明朝","serif"'>（</span></b><b><span
lang=EN-US>2</span></b><b><span style='font-family:"ＭＳ 明朝","serif"'>）卒業研究、大学院修士および博士論文修了指導人数</span></b></p>

<p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>　　　・卒業研究　　　　　</span>4<span style='font-family:"ＭＳ 明朝","serif"'>名</span></p>
<p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>　　　・大学院修士　　　　</span>8<span style='font-family:"ＭＳ 明朝","serif"'>名</span></p>
<p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>　　　・大学院博士　　　　</span>1<span style='font-family:"ＭＳ 明朝","serif"'>名</span></p>

<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>

<p class=MsoNormal><b><span style='font-family:"ＭＳ 明朝","serif"'>（</span></b><b><span
lang=EN-US>3</span></b><b><span style='font-family:"ＭＳ 明朝","serif"'>）教育業績（自己申告、テキストの作成など、授業の工夫など）</span></b></p>
<p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>&nbsp;</span></p>

<p class=MsoNormal><b><span style='font-family:"ＭＳ 明朝","serif"'>（</span><span
lang=EN-US>4</span><span style='font-family:"ＭＳ 明朝","serif"'>）国際会議出席と招待リスト</span></b></p>
<br>
<p class=MsoNormal><span lang=EN-US></span></p>

<p class=MsoNormal><b><span style='font-family:"ＭＳ 明朝","serif"'>（</span><span
lang=EN-US>5</span><span style='font-family:"ＭＳ 明朝","serif"'>）国際共同研究　(共同研究名,研究内容等)　</span></b></p>

<p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>&nbsp;</span></p>

<p class=MsoNormal><b><span style='font-family:"ＭＳ 明朝","serif"'>（</span><span
lang=EN-US>6</span><span style='font-family:"ＭＳ 明朝","serif"'>）新聞や雑誌等で報道された研究成果等　(報道媒体、報道年月日、報道内容等)</span></b></p>

<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>

<p class=MsoNormal><b><span style='font-family:"ＭＳ 明朝","serif"'>（</span>7<span style='font-family:"ＭＳ 明朝","serif"'>）国際並びに国内学会での受賞　(賞名、その内容、受賞理由等)　</span></b></p>

<p class=MsoNormal><span lang=EN-US>&nbsp;</span></p>

<p class=MsoNormal><b><span style='font-family:"ＭＳ 明朝","serif"'>（</span><span
lang=EN-US>8</span><span style='font-family:"ＭＳ 明朝","serif"'>）地域・社会と連携した教育・研究活動、学会、国、県などへの協力、など　</span></b></p>

<p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>ヨウ素学会　SIS Letters 編集委員
</span></p>

<p class=MsoNormal>　</p>

<p class=MsoNormal><b><span style='font-family:"ＭＳ 明朝","serif"'>（</span>9<span style='font-family:"ＭＳ 明朝","serif"'>）特許　(発明者名、発明の名称、出願日、出願番号、整理番号等)　</span></b></p>
<p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>&nbsp;</span></p>

<table width="698" border="1">
  <tr>
    <td width="82"><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>　整理番号</span></p></td>
    <td width="104"><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>　出願番号</span></p></td>
    <td width="61"><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>　出願日</span></p></td>
    <td width="313"><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>　　　　　　　　発明の名称</span></p></td>
    <td width="104"><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>　　発明者名</span></p></td>

    </tr>
  <tr>
    <td><p class=MsoNormal>P15-057</p></td>
    <td><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>特願<br>
2015-234304</span></p></td>
    <td><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>平成27年<br>
11月30日</span></p></td>      
    <td><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>光学活性ピロリジン触媒及びこれを用いた方法</span></p></td>
    <td><p class=MsoNormal><span style='font-family:"ＭＳ 明朝","serif"'>森山　克彦<br>
東郷　秀雄<br>
杉上　徹</span></p></td>
    </tr>
 </table><br>

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