Answers are grounded in this paper and cite their sources.
Bromine radical-mediated cyclopropylcarbinyl-homoallyl rearrangement of alkylidenecyclopropanes was effectively accomplished by C-C bond formation with allylic bromides, which led to the syntheses of 2-bromo-1,6-dienes. A three-component coupling reaction comprising alkylidenecyclopropanes, allylic bromides, and carbon monoxide also proceeded well to give 2-bromo-1,7-dien-5-ones in good yield.
No takes yet. Share an insight, caveat, or question.
Kippo et al. (2012) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: