An efficient, one‐pot, multicomponent reaction of aldehydes 1, p‐methoxyaniline (2a), and 2‐vinylindoles 3 was developed. This approach provides a practical approach to synthetically and biologically significant tetrahydro‐γ‐carboline and tetrahydroquinoline derivatives in good yields through a chemo‐ and regioselectivity switch, which can be tuned by simply changing the substituent on the indole component under identical reaction conditions.
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Cheng et al. (2010) studied this question.
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