An Efficient Synthesis of Spirocyclopropanes by [2+1] Annulation of α,β‐Unsaturated Carbonyl Compounds with Nitroacetates
Yani Peng,
Yuxin Zhang,
Minyang Wu
et al.
Abstract:An efficient synthesis of spirocyclopropanes was developed via [2+1] annulation of α,β‐unsaturated carbonyl compounds with nitroacetates. This protocol features advantages such as simple operation, broad substrate scope, high diastereoselectivity and good to excellent yields. Moreover, this work represents the first example of assembling spirocyclopropane derivatives from nitroacetates.
Small molecules, such as trimethylamine N-oxide, interrupt intramolecular photoreactions of quinones by proton transfer and allow to convert a variety of quinones to spirocyclopropanes in a catalytic, diastereoselective, and atom-conserving manner.
Small molecules, such as trimethylamine N-oxide, interrupt intramolecular photoreactions of quinones by proton transfer and allow to convert a variety of quinones to spirocyclopropanes in a catalytic, diastereoselective, and atom-conserving manner.
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