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Synthesis of New Indolizidine Derivatives from 1-(2-Quinolyl)-2-propen-1-ol
ACS Omega ( IF 3.7 ) Pub Date : 2018-03-15 00:00:00 , DOI: 10.1021/acsomega.8b00167
Donatella Giomi 1 , Jacopo Ceccarelli 1 , Alberto Brandi 1
Affiliation  

The four-step procedure involving bromination, reduction, and nucleophilic substitution via elimination/addition previously applied to 1-(2-pyridyl)-2-propen-1-ol for the synthesis of indolizidine systems has now been extended to 1-(2-quinolyl)-2-propen-1-ol allowing a general access to benzo-fused derivatives. For instance, (±)-benzo[e]lentiginosine has been easily synthesized in an 18% overall yield.

中文翻译:

1-(2-喹啉)-2-丙烯-1-醇合成新的吲哚并咪唑衍生物

以前通过将消灭/加成反应用于溴化,还原和亲核取代的四步程序(以前已应用于1-(2-吡啶基)-2-丙烯-1-醇,用于合成吲哚唑烷系统)现已扩展为1-(2 -喹啉基)-2-丙烯-1-醇,通常可使用苯并稠合衍生物。例如,很容易以18%的总收率合成(±)-苯并[ e ]龙胆草碱。
更新日期:2018-03-15
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