<p> </p> <p style="margin: 0.0px 0.0px 0.0px 0.0px; font: 10.5px 'Times New Roman'"> A user-friendly Ni-catalyzed reductive</p> <p style="margin: 0.0px 0.0px 0.0px 0.0px; font: 10.5px 'Times New Roman'"> cyclization/carboxylation of <i>unactivated </i>alkyl halides</p> <p style="margin: 0.0px 0.0px 0.0px 0.0px; font: 10.5px 'Times New Roman'"> with CO<span style="font: 7.0px 'Times New Roman'">2 </span>is described. The protocol operates under mild</p> <p style="margin: 0.0px 0.0px 0.0px 0.0px; font: 10.5px 'Times New Roman'"> conditions with excellent chemoselectivity profile and a</p> <p style="margin: 0.0px 0.0px 0.0px 0.0px; font: 10.5px 'Times New Roman'"> divergent <i>syn/anti-</i>selectivity pattern that can be easily</p> <p style="margin: 0.0px 0.0px 0.0px 0.0px; font: 10.5px 'Times New Roman'"> modulated by the substrate utilized.</p>
English
Journal of the American Chemical Society,
J. Am. Chem. Soc
info:eu-repo/grantAgreement/ERC/FP7/277883
MINECO (CTQ2012-34054)
(SEV-2013-0319)
iCIQ foundation
the European Research Council
MINECO
Severo Ochoa Excellence Accreditation
European Union
ERC, MINECO , COFUND,CELLEX
© 2015 American Chemical Society
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