A method for direct cross coupling between unactivated C(sp)-H bonds and chloroformates has been accomplished via nickel and photoredox catalysis. A diverse range of feedstock chemicals, such as (a)cyclic alkanes and toluenes, along with late-stage intermediates, undergo intermolecular C-C bond formation to afford esters under mild conditions using only 3 equiv of the C-H partner. Site selectivity is predictable according to bond strength and polarity trends that are consistent with the intermediacy of a chlorine radical as the hydrogen atom-abstracting species.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6411045 | PMC |
http://dx.doi.org/10.1021/jacs.8b09191 | DOI Listing |
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