A relay Cu(I)/Brønsted base catalyzed one‐pot phospha ‐Michael addition/5‐ exo ‐ dig cyclization/isomerization of in situ generated aza ‐alkynyl o ‐quinone methides ( N ‐ o ‐AQMs) from 1‐( o ‐aminophenyl)prop‐2‐ynols with P(O)‐compounds has been established to afford C3‐phosphorylated indoles. It demonstrates that the 1,4‐conjugate addition adduct from N ‐ o ‐AQMs could undergo further cyclization with the tethered alkyne moiety to afford N ‐heterocyclic compounds. magnified image
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Chen et al. (2021) studied this question.
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