<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Ma Y</submitter><funding>Natural Science Foundation of Zhejiang Province</funding><funding>Zhejiang Provincial Technologies R&amp;amp;D Program of China</funding><pagination>425-430</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9178507</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(5)</volume><pubmed_abstract>A series of N, P-ligands bearing carboxyl groups have been synthesized. These have been applied in conjunction with cobalt naphthenate in a facile, economic, and efficient method for the catalytic hydrosilylation of alkenes. In the presence of KO&lt;sup>t&lt;/sup>Bu as an additive, the reaction time and activation energy are greatly reduced.</pubmed_abstract><journal>Current organic synthesis</journal><pubmed_title>Carboxylate-Functionalized P, N-Ligated Cobalt Catalysts for Alkene Hydrosilylation.</pubmed_title><pmcid>PMC9178507</pmcid><funding_grant_id>LY18B020012</funding_grant_id><funding_grant_id>2017C31105</funding_grant_id><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Bai Y</pubmed_authors><pubmed_authors>Peng J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Carboxylate-Functionalized P, N-Ligated Cobalt Catalysts for Alkene Hydrosilylation.</name><description>A series of N, P-ligands bearing carboxyl groups have been synthesized. These have been applied in conjunction with cobalt naphthenate in a facile, economic, and efficient method for the catalytic hydrosilylation of alkenes. In the presence of KO&lt;sup>t&lt;/sup>Bu as an additive, the reaction time and activation energy are greatly reduced.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2025-04-04T19:06:34.323Z</modification><creation>2025-04-04T19:06:34.323Z</creation></dates><accession>S-EPMC9178507</accession><cross_references><pubmed>33319688</pubmed><doi>10.2174/1570179417666201214112514</doi></cross_references></HashMap>