Updated on 2024/10/09

Information

 

写真a

 
KAWASAKI YUYA
 
Organization
Institute for Materials Chemistry and Engineering Department of Applied Molecular Chemistry Assistant Professor
Interdisciplinary Graduate School of Engineering Sciences Department of Interdisciplinary Engineering Sciences(Concurrent)
Title
Assistant Professor
Contact information
メールアドレス
Tel
0925837809
External link

Research Areas

  • Nanotechnology/Materials / Synthetic organic chemistry

  • Nanotechnology/Materials / Structural organic chemistry and physical organic chemistry

Research History

  • 九州大学先導物質化学研究所  Assistant Professor 

    2023.4 - Present

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  • Kyushu University Institute for Materials Chemistry and Engineering Specially Appointed Assistant Professor 

    2015 - Present

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Education

  • Kyushu University   総合理工学府物質理工学専攻  

    - 2012

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Research Interests・Research Keywords

  • Research theme: development of new click reaction device

    Keyword: click chemistry, DACN

    Research period: 2016.6 - 2020.6

  • Research theme: development of effective transformation of alkyne

    Keyword: hydrosilylation, ozone oxidation

    Research period: 2014.5 - 2020.6

Awards

  • 2024年度奨励賞

    2024.9   有機合成化学協会 九州山口支部   アルキンの特性を活用した効率的分子変換法の開発と機能性分子の創製

  • 味の素 研究企画賞

    2020.2   有機合成化学協会  

Papers

  • Preparation of Enantioenriched Chiral Organic Molecules by Dynamic Asymmetric Induction from a Outer Chiral Source Invited Reviewed International journal

    Igawa, K.; Kawasaki, Y.; Ano, Y.; Kashiwagi, T.; Ogawa, K.; Hayashi, J.; Morita, R. Yoshioka, Y.; Uehara, K.; Tomooka, K.

    CHEMISTRY LETTERS   48 ( 7 )   726 - 729   2019.7

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1246/cl.190170

  • Synthesis and Stereochemical Analysis of Dynamic Planar Chiral Nine-membered Diallylic Amide:Significant Substituent Effect on Stereochemical Stability Invited Reviewed International journal

    Hayashi, J.; Uehara, K.; Ano, Y.; Kawasaki, Y.; Igawa, K.; Tomooka, K.

    Heterocycles   99   856 - 864   2019.6

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.3987/COM-18-S(F)92

  • Synthesis of NMs-DACN: Small and Hydrophilic Click Reaction Device Invited Reviewed International journal

    Kawasaki, Y.; Yamanaka, Y.; Seto, Y.; Igawa, K.; Tomooka, K.

    CHEMISTRY LETTERS   48 ( 5 )   495 - 497   2019.5

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: 10.1246/cl.190026

  • Efficient Synthesis and Structural Analysis of Chiral 4,4'-Biazulene Reviewed International journal

    Ryoji Hatakenaka, Nanami Nishikawa, Yuji Mikata, Hiroki Aoyama, Kohsuke Yamashita, Yoshihito Shiota, Kazunari Yoshizawa, Yuuya Kawasaki, Katsuhiko Tomooka, Shin Kamijo, Fumito Tani

    Chemistry - A European Journal   2024.3

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: doi.org/10.1002/chem.202400098

  • Development of DACN-NHS-ester and DACN-maleimide, and their application for the synthesis of artificial hybrid biomolecules Reviewed International journal

    Yuuya Kawasaki, Kazunobu Igawa Tomoya Hayashibara, Yuki Seto,b Yutaro Taniguchi, Katsuhiko Tomooka

    Chem. Commun.   59 ( 78 )   11724 - 11727   2023.9   ISSN:1359-7345 eISSN:1364-548X

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:Chemical Communications  

    Yuuya Kawasaki, Kazunobu Igawa,Tomoya Hayashibara, Yuki Seto, Yutaro Taniguchi, Katsuhiko Tomooka

    DOI: 10.1039/d3cc03023g

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  • Stereochemical study on planar-chiral cyclic molecules using polysaccharide-based column chromatography Reviewed International journal

    Kazunobu Igawa, Kazuhiro Uehara, Yuuya Kawasaki, Katsuhiko Tomooka

    Chirality   34   824 - 832   2022.9

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    Language:English   Publishing type:Research paper (scientific journal)  

    DOI: org/10.1002/chir.23429

  • Synthesis, Stereochemical Analysis, and Transformation of Oxa-[7] orthocyclophene

    Katsuhiko Tomooka, Chisato Iso, Yukiho Hashimoto, Masaki Suzuki, Yuuya Kawasaki, Kazunobu Igawa

    CHEMISTRY LETTERS   51 ( 7 )   788 - 790   2022.7   ISSN:0366-7022 eISSN:1348-0715

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:CHEMICAL SOC JAPAN  

    Planar chiral oxa-[7]orthocyclophene 1a was designed and synthesized with two different synthetic routes. X-ray crystallo-graphic analyses of 1a and its platinum complex revealed a highly distorted ring structure and the absolute stereochemistry of 1a, respectively. Epoxidation and [2,3]-Wittig rearrangement of 1a provided with central chiral molecules, without the loss of enantiomeric purity.

    DOI: 10.1246/cl.220219

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  • Preparation of enantioenriched helical- and axial-chiral molecules by dynamic asymmetric induction Reviewed International journal

    Kawasaki, Y.; Kamikubo, R.; Kumegawa, Y.; Ogawa, K.; Kashiwagi, T.; Ano, Y.; Igawa K.; Tomooka, K.

    Chemical Communications   58 ( 10 )   1605 - 1608   2022.6   ISSN:1359-7345 eISSN:1364-548X

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    Language:Japanese   Publishing type:Research paper (scientific journal)   Publisher:Chemical Communications  

    Dynamic asymmetric induction (DYASIN) of racemic dynamic chiral heterohelicenes afforded their highly enantioenriched forms (up to 96% ep) in quantitative yields. These heterohelicenes were readily converted into semi-static axial-chiral 1,1′-binaphthyl derivatives in a stereospecific manner.

    DOI: 10.1039/d1cc05881a

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  • Synthesis and Stereochemical Analysis of Ten-membered Diallylic Nitrogen Cycle and Its Pt-Complex

    Jun-ichi Hayashi, Masaki Suzuki, Maki Shimada, Yuuya Kawasaki, Kazunobu Igawa, Katsuhiko Tomooka

    CHEMISTRY LETTERS   51 ( 6 )   636 - 638   2022.6   ISSN:0366-7022 eISSN:1348-0715

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    Language:English   Publishing type:Research paper (scientific journal)   Publisher:CHEMICAL SOC JAPAN  

    Newly synthesized ten-membered diallylic nitrogen cycle, having E- and Z-alkene moieties, shows labile planar-chirality at ambient temperature. VT-NMR experiments revealed the detail of the stereochemical behavior of interconversion of the enantiomers and diastereomers. In sharp contrast, Pt-complex of the nitrogen cycle have more stable planar chirality, and the enantiomers of the Pt-complex were isolated by HPLC using a chiral stationary phase.

    DOI: 10.1246/cl.220143

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  • SYNTHESIS AND STEREOCHEMICAL ANALYSIS OF PLANAR CHIRAL NINE-MEMBERED AZA-ORTHOCYCLOPHYNE Reviewed International journal

    Yuuya Kawasaki, Sumire Tanaka, Kazunobu Igawa, Katsuhiko Tomooka

    HETEROCYCLES   105 ( 1 )   352 - 357   2022.4   ISSN:0385-5414

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    Language:Japanese   Publishing type:Research paper (scientific journal)   Publisher:The Japan Institute of Heterocyclic Chemistry  

    Aza-orthocyclophyne 3b with an oxy-substituent on the 16 position of the benzene ring was synthesized, and it was revealed that the stereochemical stability of 3b is consistent with the order of 1,3-steric repulsion between the C2 methylene protons and the oxy-substituent.

    DOI: 10.3987/COM-22-S(R)18

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  • Analysis of Stereochemical Stability of Dynamic Chiral Molecules Using an Automated Microflow Measurement System Reviewed

    Kazunobu Igawa, Shusaku Asano, Yuki Yoshida, Yuuya Kawasaki, Katsuhiko Tomooka

    The Journal of Organic Chemistry   86 ( 14 )   9651 - 9657   2021.7

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    Language:Others   Publishing type:Research paper (scientific journal)  

    An automated microflow measurement system for the kinetic study of racemization of dynamic chiral molecules was developed. This system facilitated the analysis of fast racemization within several seconds at elevated temperatures owing to its rapid heating ability, high performance for controlling short residence times, and ease of connection to HPLC systems for direct measurement of the enantiomeric purity. A more precise analysis was realized by combination of microflow and common batch measurements over a broad range of temperatures.

    DOI: 10.1021/acs.joc.1c00914

  • Ozone Oxidation of Silylalkene: Mechanistic Study and Application for the Synthesis of Silacarboxylic Acid Derivatives Reviewed

    Kazunobu Igawa, Yuuya Kawasaki, Sora Nozaki, Naoto Kokan, Katsuhiko Tomooka

    Journal of Organic Chemistry   85 ( 6 )   4165 - 4171   2020.3

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    Language:Others   Publishing type:Research paper (scientific journal)  

    Copyright © 2020 American Chemical Society. The addition-type ozone oxidation of silylalkenes is a highly efficient reaction to provide synthetically versatile α-silylperoxy carbonyl compounds. To gain insight into the reaction mechanism, we performed a computational study, which revealed that the reaction proceeds via [1,2]-Brook rearrangement-type silyl migration of primary ozonide. In sharp contrast to the addition-type reactions, the ozone oxidation of α-alkoxysilylalkenes proceeds in a cleavage-type manner to afford excellent yields of silacarboxylic acid esters via the 1,3-cycloelimination of primary ozonide prior to 1,2-silyl migration.

    DOI: 10.1021/acs.joc.9b03350

  • Copper‐Free Huisgen Cycloaddition for the 14‐3‐3‐Templated Synthesis of Fusicoccin‐Peptide Conjugates

    Ryoma Masuda, Yuuya Kawasaki, Kazunobu Igawa, Yoshiyuki Manabe, Hiroshi Fujii, Nobuo Kato, Katsuhiko Tomooka, Junko Ohkanda

    Chemistry – An Asian Journal   15 ( 6 )   742 - 747   2020.2

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    Language:Others   Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/asia.202000042

  • Thieme Chemistry Journals Awardees: Where Are They Now? One-Pot Synthesis of Versatile Buckle Units for Click Chemistry: 4,8-Diazacyclononynes (DACNs) Reviewed

    Kazunobu Igawa, Shin Aoyama, Yuuya Kawasaki, Takeru Kashiwagi, Yuki Seto, Runyan Ni, Naoto Mitsuda, Katsuhiko Tomooka

    SYNLETT   28 ( 16 )   2110 - 2114   2017.10

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    Language:English   Publishing type:Research paper (scientific journal)  

    Newly designed buckle units for copper-free click chemistry: 4,8-diazacyclononynes (DACNs) were efficiently synthesized with a one-pot procedure from commercially available 2-butyne-1,4-diol. The synthesized DACNs possess versatile connectors for the introduction of functional units and exhibit high click reactivity.

    DOI: 10.1055/s-0036-1588839

  • Asymmetric Ozone Oxidation of Silylalkenes Using a C-2-Symmetrical Dialkoxysilyl Group as a Chiral Auxiliary Reviewed

    Kazunobu Igawa, Yuuya Kawasaki, Kosuke Nishino, Naoto Mitsuda, Katsuhiko Tomooka

    CHEMISTRY-A EUROPEAN JOURNAL   20 ( 30 )   9255 - 9258   2014.7

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    Language:English   Publishing type:Research paper (scientific journal)  

    Ozone oxidation of silyl-substituted alkenes, namely silylalkenes, proceeds in an addition-type manner to afford alpha-silylperoxy carbonyl compounds in good to excellent yields, without the formation of normal ozonolysis products. Herein the ozone oxidation of chiral alkenylsilanes prepared from alkynes and a newly designed chiral hydrosilane is reported. The reaction affords silylperoxides with high diastereoselectivity (up to 94% d.r.). The silylperoxides are convertible into enantioenriched chiral acyloins in a stereospecific manner.

    DOI: 10.1002/chem.201402996

  • Directing Group-Controlled Hydrosilylation: Regioselective Functionalization of Alkyne Reviewed

    Yuuya Kawasaki, Youhei Ishikawa, Kazunobu Igawa, Katsuhiko Tomooka

    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY   133 ( 51 )   20712 - 20715   2011.12

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    Language:English   Publishing type:Research paper (scientific journal)  

    Pt(0)-catalyzed hydrosilylation of unsymmetric alkynes proceeds in a highly regioselective manner with a dimethylvinylsilyl (DMVS) group as the directing group. This hydrosilylation affords a single regioisomer of silylalkenes from propargylic and homopropargylic alcohol derivatives. DMVS also has an accelerating effect that allows group-selective hydrosilylation of the DMVS-attached alkyne prior to that of other alkynes. Combined hydrosilylation and transformation reactions of the resulting silylalkenes afford various tri-substituted alkenes and multi-oxy-functionalized compounds with high regioselectivity from unsymmetric alkynes.

    DOI: 10.1021/ja209553f

  • Addition-type Oxidation of Silylalkene Using Ozone: An Efficient Approach for Acyloin and Its Derivatives Reviewed

    Kazunobu Igawa, Yuuya Kawasaki, Katsuhiko Tomooka

    CHEMISTRY LETTERS   40 ( 3 )   233 - 235   2011.3

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    Language:English   Publishing type:Research paper (scientific journal)  

    Acyloins are efficiently synthesized in three steps from alkynes via hydrosilylation followed by an addition-type ozone oxidation and hydrogenation. The key intermediate alpha-silylper-oxy ketone is convertible to not only acyloin but also O-silylated acyloin and diketone.

    DOI: 10.1246/cl.2011.233

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Presentations

  • 付加型オゾン酸化反応の開発 International conference

    河崎悠也, 井川和宣, 友岡克彦

    第54回酸化反応討論会  2022.9 

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    Event date: 2022.10

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:online   Country:Japan  

  • クリック反応素子DACNの開発と応用 Invited

    河崎悠也

    第一回 臨床検体から創薬へとつなぐ リサーチユニット若手セミナー  2021.10 

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    Event date: 2021.10

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:online   Country:Japan  

  • DACN河崎悠也1,○林原智也3,鬼塚和光2 井川和宣1,3,永次史2,友岡克彦1, を用いた蛍光標識型クリック反応の開発 Invited

    河崎悠也,林原智也,鬼塚和光,井川和宣,永次史,友岡克彦

    第118回有機合成シンポジウム  2021.6 

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    Event date: 2021.6

    Language:Japanese  

    Venue:福岡   Country:Japan  

  • 動的不斉誘起 (DYASIN)による光学活性へテロヘリセンの調製 (I)

    河崎 悠也, 上久保 椋太, 小川 浩平, 柏木 健, 阿野 勇介, 井川 和宣, 友岡 克彦

    日本化学会第101回春季年会  2021.3 

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    Event date: 2021.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:online   Country:Japan  

  • 動的不斉誘起 (DYASIN)による光学活性へテロヘリセンの調製 (II)

    久米川 裕太, 上久保 椋太, 井川 和宣, 河崎 悠也, 友岡 克彦

    日本化学会 第101春季年会  2021.3 

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    Event date: 2021.3

    Language:Japanese   Presentation type:Oral presentation (general)  

    Venue:online   Country:Japan  

  • アミド置換クロモン誘導体の合成と動的立体化学挙動の解析

    井本裕樹, 河崎悠也, 井川和宣, 友岡克彦

    第36回有機合成セミナー  2019.9 

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    Event date: 2020.6

    Language:Japanese  

    Country:Japan  

  • 面不斉ジアリルアミドの立体化学的安定性に置換基と環員数が及ぼす効果

    林 純一, 河崎 悠也, 井川 和宣, 友岡 克彦

    第29回万有福岡シンポジウム  2019.5 

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    Event date: 2020.6

    Language:Japanese  

    Country:Japan  

  • 動的キラルな10員環ジアリルアミドの設計と合成,

    林 純一, 河崎 悠也, 井川 和宣, 友岡 克彦

    日本化学会第99春季年会  2019.3 

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    Event date: 2020.6

    Language:Japanese  

    Country:Japan  

  • 動的不斉誘起法(DYASIN)による光学活性キラル分子の調製

    井川和宣, 河崎悠也, 阿野勇介, 柏木健, 小川浩平, 林純一, 守田涼汰, 上久保椋太, 吉岡由香梨, 上原和浩, 友岡克彦

    第115回有機合成化学シンポジウム  2019.6 

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    Event date: 2020.6

    Language:Japanese  

    Country:Japan  

  • 生体分子の化学修飾を指向した新規クリック反応素子DACN-MMCの開発

    河崎悠也, 山中裕貴, 瀬戸祐樹, 河原慎太朗, 井川和宣, 友岡克彦

    第36回有機合成セミナー  2019.9 

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    Event date: 2019.9

    Language:Japanese  

    Country:Japan  

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MISC

  • Stereochemical study on planar‐chiral cyclic molecules using polysaccharide‐based column chromatography

    Kazunobu Igawa, Kazuhiro Uehara, Yuuya Kawasaki, Katsuhiko Tomooka

    Chirality   2022.4

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    Language:Others  

    DOI: 10.1002/chir.23429

  • Preparation of Enantioenriched Chiral Organic Molecules by Dynamic Asymmetric Induction from a Outer Chiral Source

    Kazunobu Igawa, Yuuya Kawasaki, Yusuke Ano, Takeru Kashiwagi, Kouhei Ogawa, Jun-ichi Hayashi, Ryota Morita, Yukari Yoshioka, Kazuhiro Uehara, Katsuhiko Tomooka

    Chemistry Letters   2019.7

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    Language:Others  

    DOI: 10.1246/cl.190170

  • 1,3‐ケトアミドエノラートの立体化学挙動に関する研究

    河崎悠也, 上久保椋太, 井川和宣, 友岡克彦

    日本化学会講演予稿集   2015.3

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    Language:Japanese  

    1,3‐ケトアミドエノラートの立体化学挙動に関する研究

  • オゾンによるアルケンの付加型酸化反応の開発 (研究特集 マイクロレビュー)

    井川 和宣, 河崎 悠也, 友岡 克彦

    G-COE Program Kyushu University Novel Carbon Resource Sciences newsletter   2012.7

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    Language:Japanese  

    Development of Addition-type Ozone Oxidation and Its Application

Industrial property rights

Patent   Number of applications: 0   Number of registrations: 0
Utility model   Number of applications: 0   Number of registrations: 0
Design   Number of applications: 0   Number of registrations: 0
Trademark   Number of applications: 0   Number of registrations: 0

Professional Memberships

Research Projects

  • Comprehensive analysis of bioactive proteins using phospholipid peroxide as a chemical probe

    Grant number:22K05454  2022.4 - 2025.3

    Grants-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research (C)

    安部 真人, 河崎 悠也

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    Grant type:Scientific research funding

    過酸化リン脂質は、リン脂質が酸化ストレスに晒されることで産生され、鉄イオン等の作用で二次酸化生成物を誘導する。過酸化リン脂質の作用様式は大別して、1)受容体タンパク質との相互作用、2)二次酸化生成物による酸化的修飾タンパク質の生成、が考えられる。しかし、過酸化リン脂質の受容体タンパク質および酸化的修飾タンパク質の詳細は未解明である。これに対して本研究では、過酸化リン脂質の作用点となる未発見のタンパク質の網羅的な探索に挑戦する。具体的には「過酸化リン脂質膜による受容体タンパク質のプルダウンアッセイ」と「アジド化過酸化リン脂質により生成するアジド化酸化的修飾タンパク質の可視化」の実現を目指す。

    CiNii Research

  • 多分子連結型クリック反応素子DACN-MMCの開発とそれを用いた生体分子の複合化

    Grant number:22K05097  2022 - 2024

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research (C)

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    Authorship:Principal investigator  Grant type:Scientific research funding

  • 多分子連結型クリック反応素子DACN-MMCの開発とそれを用いた生体分子の複合化

    Grant number:22K05097  2022 - 2024

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research (C)

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    Authorship:Principal investigator  Grant type:Scientific research funding

  • リン脂質カルジオリピン過酸化物の精密合成に基づくシトクロムcの遊離機構の解明

    Grant number:19K05847  2020 - 2021

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Grant-in-Aid for Scientific Research (C)

    安部 真人, 河崎 悠也

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    Authorship:Coinvestigator(s)  Grant type:Scientific research funding

    本研究では、ミトコンドリアでの活性酸素種(ROS)によるリン脂質カルジオリピン(CL)を介したシトクロムc (cyt c)漏出の分子機構解明を目指す。そのために、ROSにより産生される各種の過酸化CLおよびその二次酸化生成物の網羅的合成と過酸化部位を改変した非天然型の過酸化CLの精密合成を実現する。それらのcyt c との相互作用解析を通じた構造活性相関研究により、本研究の学術的「問い」である、“なぜCLの過酸化がcyt c との複合体を解消させるのか?”を明らかにする。

    CiNii Research

  • 生体機能分子の化学修飾を指向したクリック反応素子の開発

    2020

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    Grant type:Donation

  • 多分子連結素子DACN-MMCの開発と生体機能分子の複合化研究

    2020

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    Grant type:Donation

  • 多分子連結を可能にする新規クリック反応素子の開発とその応用

    Grant number:19K15567  2019 - 2020

    Japan Society for the Promotion of Science  Grants-in-Aid for Scientific Research  Early-Career Scientists

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    Authorship:Principal investigator  Grant type:Scientific research funding

  • 生体分子の化学修飾に有用なクリック反応素子の開発とその応用

    2019

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    Grant type:Donation

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FD Participation

  • 2020.1   Role:Participation   Title:先導研FD.

    Organizer:[Undergraduate school/graduate school/graduate faculty]

  • 2019.5   Role:Participation   Title:先導研FD.

    Organizer:[Undergraduate school/graduate school/graduate faculty]

  • 2019.1   Role:Participation   Title:先導研FD.

    Organizer:[Undergraduate school/graduate school/graduate faculty]

  • 2018.5   Role:Participation   Title:先導研FD.

    Organizer:[Undergraduate school/graduate school/graduate faculty]

  • 2018.1   Role:Participation   Title:先導研FD.

    Organizer:[Undergraduate school/graduate school/graduate faculty]

  • 2017.5   Role:Participation   Title:先導研FD.

    Organizer:[Undergraduate school/graduate school/graduate faculty]

  • 2017.1   Role:Participation   Title:先導研FD.

    Organizer:[Undergraduate school/graduate school/graduate faculty]

  • 2016.5   Role:Participation   Title:先導研FD.

    Organizer:[Undergraduate school/graduate school/graduate faculty]

  • 2016.1   Role:Participation   Title:先導研FD.

    Organizer:[Undergraduate school/graduate school/graduate faculty]

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Social Activities

  • 当研究室で開発された高機能クリック反応素子の第二弾が関東化学株式会社から製品化された.

    2020

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    当研究室で開発された高機能クリック反応素子の第二弾が関東化学株式会社から製品化された.

  • 当研究室で開発された高機能クリック反応素子の第二弾が関東化学株式会社から製品化された.

    2020

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    Type:Other

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  • 当研究室で開発された高機能クリック反応素子が関東化学株式会社から製品化された.

    2016

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    当研究室で開発された高機能クリック反応素子が関東化学株式会社から製品化された.

  • 当研究室で開発された高機能クリック反応素子が関東化学株式会社から製品化された.

    2016

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    Type:Other

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  • 九州大学先導物質化学研究所の友岡克彦教授、井川和宣助教、河崎悠也特任助教らの研究グループは、キラル分子を光学活性体として得るための新手法の開発に成功しました。これは従来の光学分割法や不斉合成法とは一線を画すものであり、光学活性なキラル医薬品やキラル機能性材料の効率的製造法としての応用が期待されます。. Newspaper, magazine

    2019.8

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    九州大学先導物質化学研究所の友岡克彦教授、井川和宣助教、河崎悠也特任助教らの研究グループは、キラル分子を光学活性体として得るための新手法の開発に成功しました。これは従来の光学分割法や不斉合成法とは一線を画すものであり、光学活性なキラル医薬品やキラル機能性材料の効率的製造法としての応用が期待されます。.

  • 九州大学先導物質化学研究所の友岡克彦教授、井川和宣助教、河崎悠也特任助教らの研究グループは、キラル分子を光学活性体として得るための新手法の開発に成功しました。これは従来の光学分割法や不斉合成法とは一線を画すものであり、光学活性なキラル医薬品やキラル機能性材料の効率的製造法としての応用が期待されます。. Newspaper, magazine

    2019.7

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    九州大学先導物質化学研究所の友岡克彦教授、井川和宣助教、河崎悠也特任助教らの研究グループは、キラル分子を光学活性体として得るための新手法の開発に成功しました。これは従来の光学分割法や不斉合成法とは一線を画すものであり、光学活性なキラル医薬品やキラル機能性材料の効率的製造法としての応用が期待されます。.