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. Author manuscript; available in PMC: 2013 Aug 19.
Published in final edited form as: J Am Chem Soc. 2013 Jul 11;135(29):10634–10637. doi: 10.1021/ja405833m

Table 2.

Scope of dual activation formal [4+3] annulationa

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a

Reactions were performed at 0.4 mmol with 1 equiv of 1, 2 equiv of 2, 0.3 equiv base, 2 equiv CsF and 2 equiv crown ether in THF (0.15 M in 1). Isolated yields of 3 are reported. Er was determined by chiral stationary-phase high performance liquid chromatography (HPLC).

b

Benzylic chloride was used for 2 instead of benzylic bromide.