Abstract
We report herein our studies on the direct photoactivation of carbonyl cyclopropanes to give biradical intermediates, leading to selective cleavage of the more substituted carbon-carbon bond. Depending on the substrate structure, extended alkenes were isolated or directly reacted in a photo-Nazarov process to give bicyclic products. Based on these results, a unified reductive ring-opening reaction was developed by using diphenyl disulfide as a HAT reagent. By performing a sequential cyclopropanation/selective ring opening reaction, we achieved a CH2 insertion into the ,- bond of both acyclic and cyclic un-saturated carbonyl compounds. Our protocol therefore provides a further tool for framework-editing of carbocycles, com-plementing the recent progress in "skeletal editing" strategies.
Supplementary materials
Title
Supplementary information
Description
General methods, experimental procedures, characterization data, computational details and copy of NMR spectra for new compounds
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Title
cartesian coordinates
Description
Cartesian coordinates of optimized structures for computation
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