| 1. |
T. Iwata, S. Kumagai, T. Yoshinaga, M. Hanada, Y. Shiota, K. Yoshizawa, M. Shindo, Quadruple Role of Pd Catalyst in Domino Reaction Involving Aryl to Alkyl 1,5-Pd Migration to Access 1,9-Bridged Triptycenes., Chem. Euro. J. accepted, 2021.06. |
| 2. |
M. Shindo, S. Makigawa, K. Kodama, H. Sugiyama, K. Matsumoto, T. Iwata, N. Wasano, A. Kano, M. T. Morita, Y. Fujii, Design and chemical synthesis of root gravitropism inhibitors: Bridged analogues of ku-76 have more potent activity, Phytochemistry 179, 112508 (2020)., 2020.06. |
| 3. |
Jun Sun, Takayuki Iwata, Mitsuru Shindo, Synthesis of 9-hydroxytriptycenes bearing a functionalized substituent at the C-10 position through a triple cycloaddition reaction of ynolates derived from 2,6-di-tert-butylphenyl esters, Chem. Lett. 49, 1084 (2020)., 2020.06. |
| 4. |
T. Iwata, T. Yoshinaga, M. Shindo, Flow synthesis of triptycene via triple cycloaddition of ynolate to benzyne, Synlett、31, 1903-1906 (2020), 2020.07. |
| 5. |
T. Iwata, T. Tomiyama, S. Fujita, and M. Shindo, First Asymmetric Total Synthesis of (-)-Isostemonamine and Kinetic Analysis of its Isomerizations, Heterocycles, 97, 712 – 718(2018)., 2018.03. |
| 6. |
S. Fujita, M. Suyama, K. Matsumoto, A. Yamamoto, T. Yamamoto, Y. Hiroshima, T. Iwata, A. Kano, Y. Shinohara, and M. Shindo, Synthesis and evaluation of simplified functionalized bongkrekic acid analogs, Tetrahedron 74, 962-969 (2018), 2018.01. |
| 7. |
S. Fujita, K. Nishikawa, T. Iwata, T. Tomiyama, H. Ikenaga, K. Matsumoto, M. Shindo, Asymmetric Total Synthesis of (-)-Stemonamine and its Stereochemical Stability, Chem. Eur. J. 24, 1539-1543 (2018), 2017.12. |
| 8. |
S. Fujimoto, K. Matsumoto, T. Iwata, M. Shindo, Aerobic Oxidative Homocoupling Reaction of Anilides Using Heterogeneous Metal Catalysts, Tetrahedron Lett. 58,973-976(2017), 2017.01. |
| 9. |
S. Umezu, G. d. P. Gomes, T. Yoshinaga, M.Sakae, K. Matsumoto, T. Iwata, I. Alabugin, M. Shindo, Regioselective One-pot Synthesis of Triptycenes via Triple-Cycloadditions of Arynes to Ynolates, Angew. Chem. Int. Ed. 56, 1298-1302 (2017), 2016.12. |
