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. 2024 Jan 4;15(6):2205–2210. doi: 10.1039/d3sc05210a

Scope of indole acetamides 2a,b.

graphic file with name d3sc05210a-u3.jpg
a

Reactions conducted on 0.4 mmol scale using 2 equiv of 2b–2o, and 1 equiv of 1a or 1s.

b

Isolated yield after chromatographic purification, Flu = 9-fuorenyl. PG = protect group.

c

N-(9H-Fluoren-9- yl)alkylanimine as the 2-azaallylprecursor.