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. Author manuscript; available in PMC: 2018 Sep 18.
Published in final edited form as: Angew Chem Int Ed Engl. 2017 Aug 17;56(39):11870–11874. doi: 10.1002/anie.201706719

Table 2.

Scope of Ni-Catalyzed Enantioselective Conjunctive Coupling[a]

graphic file with name nihms915269f5.jpg
[a]

See text and Supporting Information details. Vinyllithium prepared from n-BuLi and tetravinyl stannane. Yields are of purified material and represent the average value for two experiments.

[b]

Vinyllithium prepared from n-BuLi and vinyl iodide.

[c]

Reaction conducted at room temperature.

[d]

Substrate was (4-iodophenyl)triethylsilyl acetylene, which undergoes desilylation during oxidation.

[e]

Product difficult to oxidize; isolated as the borane after silica gel chromatography.