Affiliation:
1. Zhang Dayu School of Chemistry
2. Institute of Molecular Science and Engineering
Abstract
AbstractThe chemoselective C–C bond cleavage of bicyclo[1.1.1]pent-1-yl alcohols (BCP-OHs) was examined. Highly ring-strained BCP-OHs were found to be particularly reactive, delivering cyclobutanone derivatives through a base-mediated single C–C bond cleavage or α,β-unsaturated ketones by palladium-catalyzed dual C–C bond cleavage.
Funder
Dalian University of Technology
Cited by
2 articles.
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