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. 2019 Jan 16;141(5):1918–1922. doi: 10.1021/jacs.8b13534

Table 2. Scope of the Reductive Liebeskind–Srogl Alkylationa,b.

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a

Thioether (1 equiv, 0.2 mmol), alkyl bromide (2.0 equiv), NiBr2·diglyme (10 mol %), dppf (10 mol %), K2HPO4 (2.0 equiv), Zn (2.5 equiv), 4 Å MS, DMA (0.6 mL) at 100 °C, 6 h.

b

Isolated yields.

c

Alkyl bromide (3.0 equiv).

d

50 °C, 24 h.

e

12 h.

f

Traces of alkylation at Ph–S cleavage observed by GC-MS.