<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yang Z</submitter><funding>NIDA NIH HHS</funding><pagination>1267-70</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4309928</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>51(7)</volume><pubmed_abstract>A new domino strategy for selective synthesis of enaminones and their difluoroboron complexes through aryl migration has been developed. The reaction features low-cost and readily accessible starting materials, reliable scalability, and bond-forming efficiency as well as simple one-pot operation, which makes this strategy highly viable for future applications.</pubmed_abstract><journal>Chemical communications (Cambridge, England)</journal><pubmed_title>Synthesis of enaminones and their difluoroboron complexes through domino aryl migration.</pubmed_title><pmcid>PMC4309928</pmcid><funding_grant_id>R33 DA031860</funding_grant_id><funding_grant_id>R33DA031860</funding_grant_id><pubmed_authors>Li G</pubmed_authors><pubmed_authors>Yang Z</pubmed_authors><pubmed_authors>Tu SJ</pubmed_authors><pubmed_authors>Zhou P</pubmed_authors><pubmed_authors>Jiang B</pubmed_authors><pubmed_authors>Hao WJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis of enaminones and their difluoroboron complexes through domino aryl migration.</name><description>A new domino strategy for selective synthesis of enaminones and their difluoroboron complexes through aryl migration has been developed. The reaction features low-cost and readily accessible starting materials, reliable scalability, and bond-forming efficiency as well as simple one-pot operation, which makes this strategy highly viable for future applications.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jan</publication><modification>2020-10-29T12:56:44Z</modification><creation>2019-03-27T01:44:13Z</creation></dates><accession>S-EPMC4309928</accession><cross_references><pubmed>25475958</pubmed><doi>10.1039/c4cc08257e</doi></cross_references></HashMap>