Synthesis and Reactivity of Bicyclo[3.2.1]octanoid-Derived Cyclopropanes
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文摘
Photochemical oxa-di-蟺-methane rearrangement of bicyclo[3.2.1]octanoid scaffolds affords multifunctional, donor鈥揳cceptor cyclopropanes. A related photochemical reaction of an iminium ether substrate uncovered an unprecedented aza-di-蟺-methane rearrangement of a 尾,纬-unsaturated iminium. Donor鈥揳cceptor cyclopropanes have been evaluated as substrates for reactions generating several new chemotypes.

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