Art

J-GLOBAL ID：202002269516708547   Reference number：20A0541196

RECENT ADVANCES IN SYNTHETIC HETARYNE CHEMISTRY

合成ヘタリーン化学における最近の進歩

Author (3)： NAKAMURA Yu (Tokyo Medical and Dental Univ. (TMDU), Tokyo, JPN) ,  YOSHIDA Suguru (Tokyo Medical and Dental Univ. (TMDU), Tokyo, JPN) ,  HOSOYA Takamitsu (Tokyo Medical and Dental Univ. (TMDU), Tokyo, JPN)
Material： Heterocycles  (International Journal for Reviews and Communications in Heterocyclic Chemistry)
Volume： 98  Issue： 12  Page： 1623-1677  Publication year： Dec. 01, 2019 
JST Material Number： S0966A  ISSN： 0385-5414  CODEN： HTCYAM  Document type： Article
Article type： 文献レビュー  Country of issue： Japan (JPN)  Language： ENGLISH (EN)

Thesaurus term： chemical synthesis ,  *heterocyclic compound ,  *aromatic compound ,  *acetylenic compound ,  *reaction intermediate ,  aromatic halogen compound ,  deprotonation ,  cycloaddition ,  silylation ,  amination ,  addition reaction ,  bridged compound ,  natural material
Semi thesaurus term： aryne ,  hydroamination ,  natural material

JST classification (2)： Heterocyclic compounds in general  (CF07010Z) ,  Other natural substances of biological origin  (CF10090R)

Reference (54)：

• (a) A. Nefzi, J. M. Ostresh, and R. A. Houghten, Chem. Rev., 1997, 97, 449; (b) M. E. Welsch, S. A. Snyder, and B. R. Stockwell, Curr. Opin. Chem. Biol., 2010, 14, 347; (c) E. Vitaku, D. T. Smith, and J. T. Njardarson, J. Med. Chem., 2014, 57, 10257.
• (a) I. Osaka, S. Shinamura, T. Abe, and K. Takimiya, J. Mater. Chem. C, 2013, 1, 1297; (b) M. Stępień, E. Gońka, M. Żyła, and N. Sprutta, Chem. Rev., 2017, 117, 3479.
• (a) I. Nakamura and Y. Yamamoto, Chem. Rev., 2004, 104, 2127; (b) N. R. Candeias, L. C. Branco, P. M. P. Gois, C. A. M. Afonso, and A. F. Trindade, Chem. Rev., 2009, 109, 2703; (c) S. Cacchi and G. Fabrizi, Chem. Rev., 2011, 111, PR215; (d) J. A. Bull, J. J. Mousseau, G. Pelletier, and A. B. Charette, Chem. Rev., 2012, 112, 2642; (e) P. Majumdar, A. Pati, M. Patra, R. K. Behera, and A. K. Behera, Chem. Rev., 2014, 114, 2942; (f) B. Wu and N. Yoshikai, Org. Biomol. Chem., 2016, 14, 5402.
• (a) T. Kitamura, Aust. J. Chem., 2010, 63, 987; (b) C. M. Gampe and E. M. Carreira, Angew. Chem. Int. Ed., 2012, 51, 3766; (c) P. M. Tadross and B. M. Stoltz, Chem. Rev., 2012, 112, 3550; (d) H. Yoshida and K. Takaki, Synlett, 2012, 23, 1725; (e) H. Yoshida and K. Takaki, Heterocycles, 2012, 85, 1333; (f) D. Pérez, D. Peña, and E. Guitián, Eur. J. Org. Chem., 2013, 5981; (g) A. V. Dubrovskiy, N. A. Markina, and R. C. Larock, Org. Biomol. Chem., 2013, 11, 191; (h) A. E. Goetz, T. K. Shah, and N. K. Garg, Chem. Commun., 2015, 51, 34; (i) H. Miyabe, Molecules, 2015, 20, 12558; (j) S. Yoshida and T. Hosoya, Chem. Lett., 2015, 44, 1450; (k) J.-A. García-Loṕez and M. F. Greaney, Chem. Soc. Rev., 2016, 45, 6766; (l) F. I. M. Idiris and C. R. Jones, Org. Biomol. Chem., 2017, 15, 9044; (m) T. Roy and A. T. Biju, Chem. Commun., 2018, 54, 2580; (n) T. Matsuzawa, S. Yoshida, and T. Hosoya, Tetrahedron Lett., 2018, 59, 4197; (o) H. Takikawa, A. Nishii, T. Sakai, and K. Suzuki, Chem. Soc. Rev., 2018, 47, 8030.
• (a) P. H.-Y. Cheong, R. S. Paton, S. M. Bronner, G.-Y. J. Im, N. K. Garg, and K. N. Houk, J. Am. Chem. Soc., 2010, 132, 1267; (b) A. E. Goetz, S. M. Bronner, J. D. Cisneros, J. M. Melamed, R. S. Paton, K. N. Houk, and N. K. Garg, Angew. Chem. Int. Ed., 2012, 51, 2758; (c) A. E. Goetz and N. K. Garg, J. Org. Chem., 2014, 79, 846; (d) E. Picazo, K. N. Houk, and N. K. Garg, Tetrahedron Lett., 2015, 56, 3511; (e) S. Mirzaei and H. Khosravi, Tetrahedron Lett., 2017, 58, 3362.

Terms in the title (1)： リーン化