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. 2021 Jun 11;12(27):9466–9474. doi: 10.1039/d1sc02773e

Scope of the asymmetric cyclization of alkenyl N-propargyl ynamides 1a.

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a

Reaction conditions: 1 (0.2 mmol), Cu(MeCN)4PF6 (0.02 mmol), NaBArF4 (0.024 mmol), (S)-SEGPHOS (0.024 mmol), toluene (2 mL), 20 °C, 24 h, in Schlenk tubes; yields are those for the isolated products; ees are determined by HPLC analysis; d.r.s are determined by 1H NMR.

b

2-Me-THF as the solvent.

c

DCE as the solvent, 0 °C.

d

DCE as the solvent, 40 °C.