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Base-promoted fused β-carboline formation from 2-(1H-indol-3-yl)cyclohexan-1-ones, aldehydes and ammonium salts
A novel base-promoted fused β-carboline formation strategy from 2-(1H-indol-3-yl)cyclohexan-1-ones, aldehydes and ammonium salts has been developed. In this cascade reaction, ammonium salts served as a convenient nitrogen source and simultaneously played an important role in selectivity control, whi...
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Published in: | Organic chemistry frontiers an international journal of organic chemistry 2024-06, Vol.11 (13), p.3583-3588 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | A novel base-promoted fused β-carboline formation strategy from 2-(1H-indol-3-yl)cyclohexan-1-ones, aldehydes and ammonium salts has been developed. In this cascade reaction, ammonium salts served as a convenient nitrogen source and simultaneously played an important role in selectivity control, which can efficiently afford two different types of β-carbolines in satisfactory yields. |
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ISSN: | 2052-4110 2052-4110 |
DOI: | 10.1039/d4qo00551a |