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. Author manuscript; available in PMC: 2012 Sep 1.
Published in final edited form as: Chem Sci. 2011 Sep 1;2(9):1835–1838. doi: 10.1039/C1SC00175B

Table 1.

graphic file with name nihms322281u4.jpg
Solvent Triazolium salt Temp. (°C) Yield (%) ee (%)b drb
1c MeOH graphic file with name nihms322281t1.jpg
5
23 0 -- --
2c CHCl3 5 23 29 96 3:1:<1:<1
3d CHCl3 5 23 35 96 2:1:<1:<1
4d CHCl3 5 60 89 96 5:1:<1:<1
5d CHCl3 graphic file with name nihms322281t2.jpg
6
60 87 95 19:1:<1:<1
6d CHCl3 graphic file with name nihms322281t3.jpg
6′
60 59 93 4:1:<1:<1
a

See supporting information for general procedure.

b

Enantioselectivity and diastereoselectivity were determined by GC.

c

20 mol % Triazolium salt was added after full consumption of 2a.

d

20 mol % Triazolium salt was added at the beginning of the reaction.