<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Krasovskiy A</submitter><funding>NIGMS NIH HHS</funding><pagination>3818-21</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3365518</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>13(15)</volume><pubmed_abstract>Negishi couplings at olefinic centers do not always occur with the anticipated maintenance of stereochemistry. The source of erosion has been traced to the ligand, and a modified method has been developed that solves the stereochemical issue and significantly improves yields of Negishi couplings in general.</pubmed_abstract><journal>Organic letters</journal><pubmed_title>Ligand effects on Negishi couplings of alkenyl halides.</pubmed_title><pmcid>PMC3365518</pmcid><funding_grant_id>R01 GM086485</funding_grant_id><pubmed_authors>Krasovskiy A</pubmed_authors><pubmed_authors>Lipshutz BH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Ligand effects on Negishi couplings of alkenyl halides.</name><description>Negishi couplings at olefinic centers do not always occur with the anticipated maintenance of stereochemistry. The source of erosion has been traced to the ligand, and a modified method has been developed that solves the stereochemical issue and significantly improves yields of Negishi couplings in general.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Aug</publication><modification>2025-04-04T23:29:45.603Z</modification><creation>2019-03-27T00:54:03Z</creation></dates><accession>S-EPMC3365518</accession><cross_references><pubmed>21739948</pubmed><doi>10.1021/ol2010165</doi></cross_references></HashMap>