Skip to main content
. Author manuscript; available in PMC: 2015 Feb 1.
Published in final edited form as: Nat Commun. 2014 Aug 1;5:4455. doi: 10.1038/ncomms5455

Table 3.

a Variations in Vinylic Substitution.

graphic file with name nihms-607085-f0018.jpg
entry comp'd product yield, %b drc ee, %d
1 a graphic file with name nihms-607085-t0019.jpg 87 >97:3 99
2 b graphic file with name nihms-607085-t0020.jpg 85 >97:3 99
3 c graphic file with name nihms-607085-t0021.jpg 86 >97:3 99
4 d graphic file with name nihms-607085-t0022.jpg 89 >97:3 99
a

Reaction conducted with 23 (0.50 mmol, 1.0 equiv), 6 (0.60 mmol, 1.2 equiv) or 22 (1.0 mmol, 2.0 equiv) and Rh2(R-DOSP)4 (0.0005 mmol, 0.1 mol %), unless otherwise indicated.

b

Isolated yield of the major diastereomer.

c

Determined by 1H NMR analysis of the crude reaction residue.

d

Determined by HPLC analysis on a chiral stationary phase.