Skip to main content
. 2021 Sep 20;12(40):13398–13403. doi: 10.1039/d1sc04047b

Substrate scopea,b,c,d.

graphic file with name d1sc04047b-u2.jpg
a

Reaction conditions: allylboronate (±)-3 (0.3 mmol, 3.0 equiv.), aldehyde (0.1 mmol, 1.0 equiv.), (S)-A (5 mol%), 4 Å molecular sieves, toluene, −45 °C; then NaOH, H2O2, 0 °C.

b

Z/E-selectivities were determined by 1H NMR analysis of the crude reaction products.

c

Yields of isolated products 4 are listed.

d

Enantiopurities of 4 were determined by HPLC analysis.

e

The reactions were conducted with 10 mol% of (S)-A.