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. Author manuscript; available in PMC: 2016 Nov 10.
Published in final edited form as: J Am Chem Soc. 2016 Jun 22;138(26):8084–8087. doi: 10.1021/jacs.6b04818

Table 2.

Photoredox-Enabled Csp3–Csp2 Coupling from Alkyl and Aryl Halide Precursors: Comprehensive Scope of Productsa

graphic file with name nihms827728f3.jpg
a

All yields are isolated yields using photocatalyst 1 (1 mol %), NiCl2·dtbbpy (0.5 mol %), aryl halide (0.5 mmol), alkyl halide (0.75 mmol), TTMSS

(0.5 mmol), and Na2CO3 (2 equiv).

b

12 h

c

LiOH as base.

d

Aryl chloride.

e

10 mol % 2.

f

5 mol % 2.

g

MOMCl.

h

MeOTs and LiBr.

i

Dioxane as solvent.

j

48 h.

k

24 h.