SYNTHESIS OF SUBSTITUTED t-BUTYL 3-ALKYLOXINDOLE-3-CARBOXYLATES FROM DI-t-BUTYL (2-NITROPHENYL)MALONATES

YAMAI Yu-suke; TANAKA Akio; YAJIMA Tatsuo; ISHIDA Kyoji; NATSUTANI Itaru; UESATO Shinichi; NAGAOKA Yasuo; SUMIYOSHI Takaaki

Art

J-GLOBAL ID：201902260892380129 Reference number：19A0152860

SYNTHESIS OF SUBSTITUTED t-BUTYL 3-ALKYLOXINDOLE-3-CARBOXYLATES FROM DI-t-BUTYL (2-NITROPHENYL)MALONATES

(2-ニトロフェニル)マロン酸ジ-t-ブチルからの置換3-アルキルオキシンドール-3-カルボン酸t-ブチルの合成

Publisher site {{ this.onShowPLink() }} Copy service {{ this.onShowCLink("http://jdream3.com/copy/?sid=JGLOBAL&noSystem=1&documentNoArray=19A0152860&COPY=1") }}
Access JDreamⅢ for advanced search and analysis. {{ this.onShowJLink("http://jdream3.com/lp/jglobal/index.html?docNo=19A0152860&from=J-GLOBAL&jstjournalNo=S0966A") }}

Author (8)： , , , , , , ,
Material：
Volume： 97 Issue： 1 Page： 192-210 Publication year： Sep. 01, 2018
JST Material Number： S0966A ISSN： 0385-5414 CODEN： HTCYAM Document type： Article
Article type：原著論文 Country of issue： Japan (JPN) Language： ENGLISH (EN)

, , , , , , , , , , ,
,

Condensed derivatives of pyrroles

, , , , , , , ,

Reference (20)：

For recent reviews, see: a) M. M. M. Santos, Tetrahedron, 2014, 70, 9735; b) B. M. Trost and M. K. Brennan, Synthesis, 2009, 3003; c) S. Peddibhotla, Curr. Bioact. Compd., 2009, 5, 20; d) C. V. Galliford and K. A. Scheidt., Angew. Chem. Int. Ed., 2007, 46, 8748; e) H. Lin and S. J. Danishefsky, Angew. Chem. Int. Ed., 2003, 42, 36; f) C. Marti and E. M. Carreira, Eur. J. Org. Chem., 2003, 2209.
Recent examples, copper-catalyzed intramolecular dehydrogenative coupling, see: a) S. I. Son, W. K. Lee, J. Choi, and H.-J. Ha, Green Chem., 2015, 17, 3306; b) P. Drouhin, T. E. Hurst, A. C. Whitwood, and R. J. K. Taylor, Tetrahedron, 2015, 71, 7124; c) J.-S. Tang and C.-C. Guo, Synthesis, 2015, 47, 108; Transition-metal-free synthesis, see: d) N. Kumar, S. Ghosh, S. Bhunia, and A. Bisai, Beilstein J. Org. Chem., 2016, 12, 1153; e) B. Mondal and B. Roy, RSC Adv., 2015, 5, 69119; 1,2-Rearrangement, see: f) X. Jiang, J. Yang, F. Zhang, P. Yu, P. Yi, Y. Sun, and Y. Wang, Org. Lett., 2016, 18, 3154; Alkylation, see: g) S. Mizuta, K. Kitamura, K. Nishi, R. Hashimoto, T. Usui, and K. Chiba, RSC Adv., 2016, 6, 43159; Tandem reduction-lactamization, see: h) B. Nammalwar, R. A. Bunce, and J. T. Hiett, Org. Prep. Proced. Int., 2015, 47, 338; i) L. Zhang, T. Yang, X. Xie, and G. Liu, Bioorg. Med. Chem. Lett., 2015, 25, 2937.
Palladium-catalyzed C-C coupling, see: K. Soai, S. Yokoyama, T. Hayasaka, and K. Ebihara, J. Org. Chem., 1988, 53, 4149.
Copper-catalyzed intramolecular dehydrogenative coupling, see: a) T. E. Hurst, R. M. Gorman, P. Drouhin, A. Perry, and R. J. K. Taylor, Chem. Eur. J., 2014, 20, 14063; b) D. S. Pugh and R. J. K. Taylor, Org. Synth., 2012, 89, 438; c) J. E. M. N. Klein, A. Perry, D. S. Pugh, and R. J. K. Taylor, Org. Lett., 2010, 12, 3446; d) D. S. Pugh, J. E. M. N. Klein, A. Perry, and R. J. K. Taylor, Synlett, 2010, 934; e) A. Perry and R. J. K. Taylor, Chem. Commun., 2009, 3249.
Transition-metal-free synthesis, see: a) D. Dey, S. Ghosh, and D. Chopra, J. Chem. Crystallogr., 2014, 44, 131; b) S. Bhunia, S. Ghosh, D. Dey, and A. Bisai, Org. Lett., 2013, 15, 2426; c) S. Ghosh, S. De, B. N. Kakde, S. Bhunia, A. Adhikary, and A. Bisai, Org. Lett., 2012, 14, 5864; d) J. Liang, J. Chen, F. Du, X. Zeng, L. Li, and H. Zhang, Org. Lett., 2009, 11, 2820.

ｍore...

, , ,

Return to Previous Page