| 1. |
Mizuki Hyodo, Takayuki Iwata, Shindo Mitsuru, Synthesis of iptycenes Using Ambident Anthracene, 日本化学会第102春季年会, 2022.03. |
| 2. |
Mitsuru Shindo, Generation and reactions of lithium ynolates: Regioselective one-pot synthesis of triptycenes, Pacifichem2021, 2021.12. |
| 3. |
Takayuki Iwata, ＃Yusuke Maehata, ＃Tatsuro Yoshinaga, Mitsuru Shindo,, Synthesis of macrocyclic compounds using 1,8,13-substituted triptycenes as a foundation,, The 4th IRCCS International Symposium, 2021.03. |
| 4. |
優秀発表賞. |
| 5. |
岩田 隆幸・＃藤田 聡・＃富山 泰至・＠松本 健司・＠平尾 雅代・＠竹田 修三・新藤 充, ステモナアルカロイドの不斉全合成、異性化解析および乳がん細胞死滅作用, 日本化学会第99春季年会, 2019.03. |
| 6. |
Mitsuru Shindo, Takayuki Iwata, Arihiro Kano, Yoshiharu Fujii,, Studies on Plant Root Gravitropism Inhibitors Derived from Allelochemical,, The 1st International Symposium on Chemical Communication (ISCC2019),, 2019.01. |
| 7. |
Takayuki Iwata, Tatusro Yoshinaga, Satoshi Umezu, Takumi Fujiwara, Mikei Sakae, Kenji Matsumoto, Mitsuru Shindo, Regioselective Synthesis of Substituted Triptycenes Using Ynolate-aryne Triplecycloadditions, The 14th International Kyoto Conference on New Aspects of Organic Chemistry, IKCOC-14, 2018.11. |
| 8. |
＃Furusawa、Y., ＃, Sun, J., Iwata, T., Shindo, M.,, Synthesis of Molecular Probes of Cis-Cinnamic Acid Analog with Antigravitropic Activity, 4th International Conference of Asian Allelopathy Society, 2018.09, アレロパシー活性化合物の分子イメージング実験から得られた結果を元に、新規植物重力屈性阻害化合物の開発に成功し、さらにその分子蛍光プローブを合成し、その分子イメージング実験により局在部位に関する情報を得た。. |
| 9. |
＃李穎, 岩田隆幸, 狩野有宏, 岩田隆幸、新藤充, Synthesis and Evaluation of Glucose Conjugates of Bongkrekic Acid analogs, 第55回化学関連支部合同九州大会, 2018.06. |
| 10. |
T. Yoshinaga, T. Fujiwara, T. Iwata, M. Shindo,, Synthesis of distorted triptycenes using ynolate-aryne triple cycloaddition and their transformations,, 2018 IMCE International Symposium, 2018.03. |
| 11. |
J. Gong, M. Kamita, M. Shindo, A. Kano,, Role of M-CSF expressed form 4T1 tumor cells in immune activation, 2018 IMCE International Symposium, 2018.03. |
| 12. |
M. Shindo, Regioselective One-pot Synthesis of Triptycenes via Triple Cycloaddition of Arynes to Ynolates,, The 12th International Conference on Cutting-Edge Organic Chemistry in Asia (ICCEOCA-12), 2017.11. |
| 13. |
Li Ying, Donha Choi, Takayuki Iwta, Arihiro Kano, Mitsuru Shindo, 348. Synthesisi of Glucose Conjugates of Bongkrekic acid analogue for Enhancing Cell Permeability, 第２９回若手研究者のためのセミナー, 2017.08. |
| 14. |
藤田聡, 西川 慶祐, 池永大, 松本 健司, 岩田 隆幸, 新藤 充, Total Synthesis of (-)-Stemonamine, Junior ICCEOCA-6 , 2016.10. |
| 15. |
新藤 充, 和宇慶久, 松尾和真, 松本 健司, Cu(II)-catalyzed Dissymmetrization of Dithiomalonates, Pacifichem2015, 2015.12. |
| 16. |
松本 健司, 堂籠 健斗, 新藤 充, Heterogeneous Rh-catalyzed Oxidative Coupling of Arylamines, XXVI International Conference on Organometallic Chemistry, ICOMC2014, 2014.07. |
| 17. |
新藤 充, Total Synthesis of Stemonamine, ISIS-8, 2013.11. |
| 18. |
新藤 充, Reactions of Ynolates and Synthetic Applications, 10th International Symposium on Carbanion Chemistry, 2013.09, イノラートの生成と合成的応用について講演した. |
| 19. |
新藤 充, Olefination Controlled by Torquoselectivity, Nang Young Technological University organic chemistry symposium, 2013.01. |
| 20. |
新藤 充, Total Synthesis of Stemonamine, Cambodian Maleysian Chemical Congress, 2012.10. |
| 21. |
新藤 充, 寺井やすあき, 行平大地, 三浦 大典, 藤村 由紀, 松本 健司, 割石 博之, Design and synthesis of new efficient MALDI-MS matrices for low molecular weight metabolites in negative ionization mode, 19th International Mass Specrometry Conference (IMSC2012, 2012.09. |
| 22. |
Catalytic Nazarov Reaction. |
| 23. |
Torquoselective Olefination. |
| 24. |
Highly stereoselective olefination using ynolates. |
| 25. |
Regioselective nazafov cyclization with rearrangement of alkoxy group. |
| 26. |
Total Synthesis of Sundiversifolide. |
| 27. |
One-pot synthesis of multisubstituted furans via ynolates,. |
| 28. |
Synthetic studies of sundiversifolide. |
| 29. |
The Coupling reaction of trialkylvinylsilanes and vinylgermanes using activation by hypervalency. |
| 30. |
Synthetic Study of Sundiversifolide. |
| 31. |
Stereocontrolled Syntheses of multisubstituted (E)- and (Z)-olefins via ynolates utilyzing silicone and germanium. |
