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Abstract:
The direct C-H functionalization of tetrahydro-γ-carbolines (THγCs) at the α-position has been presented. This mild and simple strategy allows coupling of THγCs with various anilines and indoles with satisfactory to excellent yields. This two-step/one-pot method could be applied to synthesize complex compounds and is suitable for the C-H functionalization of similar biologically active structures. © 2022 The Royal Society of Chemistry.
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New Journal of Chemistry
ISSN: 1144-0546
Year: 2022
Issue: 20
Volume: 46
Page: 9511-9514
3 . 3
JCR@2022
2 . 7 0 0
JCR@2023
ESI HC Threshold:74
JCR Journal Grade:2
CAS Journal Grade:3
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ESI Highly Cited Papers on the List: 0 Unfold All
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30 Days PV: 1
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