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. 2020 Apr 20;16:778–790. doi: 10.3762/bjoc.16.71

Table 3.

Substrate scope of the reaction with indoles.a

graphic file with name Beilstein_J_Org_Chem-16-778-i033.jpg

Indoles Trifluoromethly substituted hydroxylakylated indoles Mp (°C) Purity (%)b Yield (%)c

Inline graphic
1b
Inline graphic
3p
122–124
(75)d [25]
98 96
(95)e [25]
Inline graphic
1c
Inline graphic
3q
160–161 99 79
Inline graphic
1d
Inline graphic
3r
192–193 97 90
Inline graphic
1e
Inline graphic
3s
112–113 99 94
(98)e [24]
Inline graphic
1f
Inline graphic
3t
90–91
(90)d [24]
99 96
(98)e [24]
Inline graphic
1g
Inline graphic
3u
165–166 98 91
Inline graphic
1h
Inline graphic
3v
227–228 97 92
Inline graphic
1i
Inline graphic
3w
239–240 99 97
Inline graphic
1j
Inline graphic
3x
185–186
185d [24]
97 90
86e [24]

aReaction conditions: 1 (3.4 mmol) and 2 (3.75 mmol) in water (5 mL). bPurity was determined by HPLC coupled to a UV diode array detector (DAD) at 220−400 nm. cIsolated yields. dReported melting points. eReported yields.