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. Author manuscript; available in PMC: 2011 Jul 28.
Published in final edited form as: J Am Chem Soc. 2010 Jul 28;132(29):10015–10017. doi: 10.1021/ja104313x

Table 3.

Enantioselective Cascade Cycloaddition: Olefin Scopea,b

graphic file with name nihms219111t3.jpg
a

Results listed as product, yield, diastereomeric ratio (dr), enantiomeric excess (% ee).

b

Diastereomeric ratio, % ee determined as in Table 1.

c

Reaction conducted at −20 °C.

d

Reaction performed with Fe(phen)3(PF6)3 as oxidant.

e

Reaction conducted at −40 °C.