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. Author manuscript; available in PMC: 2019 Nov 21.
Published in final edited form as: J Am Chem Soc. 2018 Nov 5;140(46):15943–15949. doi: 10.1021/jacs.8b10008

Table 2.

Stereospecific [2+2] Cycloadditions

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a

Determination by 1H NMR of the crude reaction mixture utilizing a calibrated standard. Reactions run under optimized conditions using catalyst 2e.

b

Yields reported of pure major isomer as average of two experiments.

c

Enantiomeric ratio of the major isomer (see Supporting Information for er of minor isomers).

d

Reactions run at −20 °C.

e

Combined yield of both isomers in parentheses.