<HashMap><database>biostudies-other</database><scores/><additional><omics_type>Unknown</omics_type><volume>7</volume><submitter>Bonnafoux L</submitter><journal>Beilstein journal of organic chemistry</journal><pagination>1278-87</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3182437</full_dataset_link><abstract>Regioselective bromine-lithium exchange reactions on polybrominated biaryls enable the modular synthesis of various polysubstituted biphenyls such as bis(dialkylphosphino)-, bis(diarylphosphino)- and dialkyl(diaryl)phosphinobiphenyls. All permutations of substituents at the ortho positions of the biphenyls are possible. In a similar manner, one can gain access to monophosphine analogues. So far, such a process, based on the effective discrimination between bromine atoms as a function of their chemical environment, has been observed only sporadically.</abstract><repository>biostudies-other</repository><pmcid>PMC3182437</pmcid><data_source>Europe PMC</data_source><pubmed_authors>Bonnafoux L</pubmed_authors><pubmed_authors>Leroux FR</pubmed_authors><pubmed_authors>Colobert F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bromine-lithium exchange: An efficient tool in the modular construction of biaryl ligands.</name><description>Regioselective bromine-lithium exchange reactions on polybrominated biaryls enable the modular synthesis of various polysubstituted biphenyls such as bis(dialkylphosphino)-, bis(diarylphosphino)- and dialkyl(diaryl)phosphinobiphenyls. All permutations of substituents at the ortho positions of the biphenyls are possible. In a similar manner, one can gain access to monophosphine analogues. So far, such a process, based on the effective discrimination between bromine atoms as a function of their chemical environment, has been observed only sporadically.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 </publication><modification>2019-03-26T22:30:21Z</modification><creation>2019-03-26T22:30:21Z</creation></dates><accession>S-EPMC3182437</accession><cross_references><pubmed>21977212</pubmed><doi>10.3762/bjoc.7.148 </doi></cross_references></HashMap>