Fig. 3: Substate scope of silyl dienol ethers and BCBs. | Nature Communications

Fig. 3: Substate scope of silyl dienol ethers and BCBs.

From: Facile access to bicyclo[2.1.1]hexanes by Lewis acid-catalyzed formal cycloaddition between silyl enol ethers and bicyclo[1.1.0]butanes

Fig. 3

aReaction conditions: unless indicated otherwise, the reaction of silyl dienol ether 1 (0.2 mmol), and BCB 2 (0.26 mmol) was carried out in DCM (2 mL) or toluene (2 mL) in the presence of Yb(OTf)3 (0.01 mmol) at room temperature for 3 h. The yield was of isolated and purified products. bThe reaction was run in the presence of Sc(OTf)3 (0.02 mmol) at room temperature for 30 min. rr: regioselectivity ratio of (4 + 3) to (3 + 2) cycloadduct. Naph 2-naphthyl, TIPS triisopropylsilyl.

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