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- W2803982497 abstract "An efficient approach for the synthesis of functionalized tetrahydro-pyrido/quinolinocarbazoles from 2-alkynylindole-3-carbaldehydes and l-proline utilizing a metal-free decarboxylative cyclization, ring expansion, and ring contraction strategy via the generation of azomethine ylide was developed. The reaction of 2-alkynylindole-3-carbaldehydes with l-thioproline leads to the formation of γ-carbolines. By virtue of this expedient method, a diverse range of biologically active heteroannulated carbazoles can be synthesized efficiently." @default.
- W2803982497 created "2018-06-01" @default.
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- W2803982497 date "2018-05-23" @default.
- W2803982497 modified "2023-09-27" @default.
- W2803982497 title "Transition-Metal-Free Access to Pyridocarbazoles from 2-Alkynylindole-3-carbaldehydes via Azomethine Ylide" @default.
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- W2803982497 doi "https://doi.org/10.1021/acs.joc.8b00980" @default.
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