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. 2016 Mar 8;7(7):4105–4109. doi: 10.1039/c6sc00702c

Table 3. Evaluation of nucleophile scope a .

graphic file with name c6sc00702c-u5.jpg
graphic file with name c6sc00702c-u6.jpg

aIsolated yields and ee's are the average of two runs on a 0.5 mmol scale with 3 equiv. RZnBr.

bReaction was run with 20 mol% Ni(acac)2 and 24 mol% L3.

cReaction was run with RZnI.

dYield and ee determined after Pd/C-catalyzed hydrogenation to the piperidine.

eReaction was run with 1.25 equiv. i-BuOCOCl.

fReaction was run from –78 °C → rt.