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. 2014 Aug 26;10:1991–1998. doi: 10.3762/bjoc.10.207

Table 3.

Synthesis of 2-allyltryptophans 3k–o.a

graphic file with name Beilstein_J_Org_Chem-10-1991-i023.jpg

Entry Indole Tryptophan Time (h) Yield (%)b

1 Inline graphic
1k
Inline graphic
3k
48 61
2 Inline graphic
1l
Inline graphic
3l
16 86
3 Inline graphic
1m
Inline graphic
3m
16 70
4 Inline graphic
1n
Inline graphic
3n
72 NR
5 Inline graphic
1o
Inline graphic
3o
48 68

aReaction conditions: 1k–o (0.25 mmol), 2a (0.3 mmol), EtAlCl2 (0.5 mmol), CH2Cl2 (2.5 mL), rt. bYields of the isolated products after column chromatography. NR, no reaction.