当前位置:
X-MOL 学术
›
Heterocycles
›
论文详情
Our official English website, www.x-mol.net, welcomes your
feedback! (Note: you will need to create a separate account there.)
Synthesis of Pyrrolo[2,3-C]Quinoline Alkaloid Marinoquinolines
Heterocycles ( IF 0.8 ) Pub Date : 2020-06-23 , DOI: 10.3987/com-20-s(k)14 Tominari Choshi , Takashi Nishiyama , Mari Murakami , Kimiko Taninaka , Erina Hamada , Daiki Kinou , Noriyuki Hatae , Mai Endo
Heterocycles ( IF 0.8 ) Pub Date : 2020-06-23 , DOI: 10.3987/com-20-s(k)14 Tominari Choshi , Takashi Nishiyama , Mari Murakami , Kimiko Taninaka , Erina Hamada , Daiki Kinou , Noriyuki Hatae , Mai Endo
In this study, the synthesis of pyrrolo[2,3-c]quinoline as a common skeleton, is described. The process is based on the thermal electrocyclization of 3-phenylpyrrole containing isocyanate as 2-azahexatriene. Using this approach, the total synthesis of three natural marinoquinolines A, B, and E can be successfully achieved.
中文翻译:
吡咯并[2,3-C]喹啉生物碱Marinoquinolines的合成
在这项研究中,描述了作为常见骨架的吡咯并[2,3- c ]喹啉的合成。该方法基于含有异氰酸酯作为2-氮杂己三烯的3-苯基吡咯的热电环化。使用这种方法,可以成功地完成三种天然马林喹啉A,B和E的全合成。
更新日期:2020-06-23
中文翻译:
吡咯并[2,3-C]喹啉生物碱Marinoquinolines的合成
在这项研究中,描述了作为常见骨架的吡咯并[2,3- c ]喹啉的合成。该方法基于含有异氰酸酯作为2-氮杂己三烯的3-苯基吡咯的热电环化。使用这种方法,可以成功地完成三种天然马林喹啉A,B和E的全合成。