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. Author manuscript; available in PMC: 2016 Dec 12.
Published in final edited form as: J Am Chem Soc. 2016 Oct 25;138(43):14226–14229. doi: 10.1021/jacs.6b09649

Table 3.

Evaluation of trisubstituted alkenols

graphic file with name nihms-834668-t0012.jpg
a

Yields are reported as an average of two parallel experiments. Enantioselectivity determined by SFC or GC equipped with a chiral column. Reaction performed on 0.25 mmol scale.

b

7.5 mol % of Pd2dba3•CHCl3, 16 mol % L2, 2 equivalents of alkenol added and the reaction stirred for 56 hours.