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               <dc:title>Exploring benzylic gem-C(sp3)–boron–silicon and boron–tin centers as a synthetic platform</dc:title>
               <dc:creator>Chen, Wei W.</dc:creator>
               <dc:creator>Pipaon Fernández, Nahiane</dc:creator>
               <dc:creator>Díaz Baranda, Marta</dc:creator>
               <dc:creator>Cunillera, Anton</dc:creator>
               <dc:creator>Rodríguez González, Laura</dc:creator>
               <dc:creator>Shafir, Alexandr</dc:creator>
               <dc:creator>Cuenca, Ana Belen</dc:creator>
               <dc:subject>Enllaços químics</dc:subject>
               <dc:subject>Bor</dc:subject>
               <dc:subject>Silici</dc:subject>
               <dc:description>A stepwise build-up of multi-substituted Csp3 carbon centers is an attractive, conceptually simple, but often synthetically challenging type of disconnection. To this end, this report describes how gem-α,α-dimetalloid-substituted benzylic reagents bearing boron/silicon or boron/tin substituent sets are an excellent stepping stone towards diverse substitution patterns. These gem-dimetalloids were readily accessed, either by known carbenoid insertion into C–B bonds or by the newly developed scalable deprotonation/metallation approach. Highly chemoselective transformations of either the C–Si (or C–Sn) or the C–B bonds in the newly formed gem-Csp3 centers have been achieved through a set of approaches, with a particular focus on exploiting the synthetically versatile polarity reversal in organometalloids by λ3-aryliodanes. Of particular note is the metal-free arylation of the C–Si (or C–Sn) bonds in such gem-dimetalloids via the iodane-guided C–H coupling approach. DFT calculations show that this transfer of the (α-Bpin)benzyl group proceeds via unusual [5,5]-sigmatropic rearrangement and is driven by the high-energy iodine(III) center. As a complementary tool, the gem-dimetalloid C–B bond is shown to undergo a potent and chemoselective Suzuki–Miyaura arylation with diverse Ar–Cl, thanks to the development of the reactive gem-α,α-silyl/BF3K building blocks.</dc:description>
               <dc:date>2021-07-02</dc:date>
               <dc:type>info:eu-repo/semantics/article</dc:type>
               <dc:identifier>2041-6539</dc:identifier>
               <dc:identifier>http://hdl.handle.net/20.500.14342/4075</dc:identifier>
               <dc:identifier>http://dx.doi.org/10.1039/d1sc01741a</dc:identifier>
               <dc:language>eng</dc:language>
               <dc:relation>Chemical Science</dc:relation>
               <dc:relation>https://www.rsc.org/suppdata/d1/sc/d1sc01741a/d1sc01741a1.pdf</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/MINECO/PN I+D/CTQ2017-85378-R</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/MICINN/PN I+D/PID2020-113661GB-I00</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/SUR del DEC/SGR/2017 SGR 01051</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/SUR del DEC/SGR/2017 SGR 00294</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/URL/Projectes recerca PDI/2019-URL_Proj-034</dc:relation>
               <dc:relation>info:eu-repo/grantAgreement/URL i La Caixa/Projectes recerca PDI/2017-URL-Intermac-010</dc:relation>
               <dc:relation>Supplementary information</dc:relation>
               <dc:rights>http://creativecommons.org/licenses/by-nc/4.0/</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
               <dc:rights>© L'autor/a</dc:rights>
               <dc:rights>Attribution-NonCommercial 4.0 International</dc:rights>
               <dc:publisher>Royal Society of Chemistry</dc:publisher>
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