Synthesis of Fluorinated Pyrrolo[2,1- a ]isoquinolines through Decarboxylative/Dehydrofluorinative [3 + 2] Cycloaddition Aromatization of Isoquinolinium N -Ylides with Difluoroenoxysilanes.
Wenxue XiYiheng ZhangHaijian WuJinshan LiYurong WangJianguo YangZhiming WangWeijun YaoPublished in: Organic letters (2023)
A decarboxylative/dehydrofluorinative formal [3 + 2] cycloaddition aromatization of isoquinolinium N -ylides with difluoroenoxysilanes has been developed. This methodology provides a facile and straightforward synthetic pathway to afford highly functionalized fluorinated pyrrolo[2,1- a ]isoquinolines in good to excellent yields under mild conditions. Moreover, gram-scale and synthetic derivatization experiments for the late-stage functionalization of drug molecules have also been demonstrated.
Keyphrases
- visible light
- quantum dots
- ms ms
- gram negative
- liquid chromatography tandem mass spectrometry
- high performance liquid chromatography
- simultaneous determination
- gas chromatography mass spectrometry
- reduced graphene oxide
- emergency department
- tandem mass spectrometry
- solid phase extraction
- multidrug resistant
- gas chromatography
- high resolution
- gold nanoparticles