<div> <p> A Ni-catalyzed reductive carboxylation technique en route to cyclopropyl carboxylic acids has been developed. This user-friendly and mild transformation operates at atmospheric pressure of CO <sub>2 </sub>and utilizes either organic halides or alkene precursors, thus representing the first example of catalytic reductive carboxylation of secondary counterparts lacking adjacent p-components.</p> </div> <p> </p>
Anglès
Nickel, carboxylation; cross-coupling; carbon dioxide; catalysis
Synthesis
info:eu-repo/grantAgreement/ERC/FP7/277883
MINECO (CTQ2012-34054
Severo Ochoa Excellence Accreditation 2014-2018, SEV-2013-0319
the European Research Council (ERC-277883)
MINECO (CTQ2012-34054
Severo Ochoa Excellence Accreditation 2014-2018
Cellex Foundat
the European Research Council (ERC-277883), MINECO (CTQ2012-34054 & Severo Ochoa Excellence Accreditation 2014-2018, SEV-2013-0319) and Cellex Foundat
© Georg Thieme Verlag Stuttgart · New York
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