<HashMap><database>biostudies-other</database><scores/><additional><submitter>Smith CR</submitter><funding>NIGMS NIH HHS</funding><pagination>1169-71</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3384527</full_dataset_link><abstract>Indolizine, pyrrolone, and indolizinone heterocycles are easily accessed via the Pt(II)-catalyzed cycloisomerization or a tandem cyclization/1,2-migration of pyridine propargylic alcohols and derivatives. This method provides an efficient synthesis of highly functionalized heterocycles from readily available substrates. [reaction: see text]</abstract><repository>biostudies-other</repository><data_source>Europe PMC</data_source><omics_type>Unknown</omics_type><volume>9(6)</volume><journal>Organic letters</journal><pmcid>PMC3384527</pmcid><funding_grant_id>R01 GM084906</funding_grant_id><pubmed_authors>Rhodes AJ</pubmed_authors><pubmed_authors>Smith CR</pubmed_authors><pubmed_authors>Bunnelle EM</pubmed_authors><pubmed_authors>Sarpong R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pt-catalyzed cyclization/1,2-migration for the synthesis of indolizines, pyrrolones, and indolizinones.</name><description>Indolizine, pyrrolone, and indolizinone heterocycles are easily accessed via the Pt(II)-catalyzed cycloisomerization or a tandem cyclization/1,2-migration of pyridine propargylic alcohols and derivatives. This method provides an efficient synthesis of highly functionalized heterocycles from readily available substrates. [reaction: see text]</description><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Mar</publication><modification>2019-03-27T00:55:00Z</modification><creation>2019-03-27T00:55:00Z</creation></dates><accession>S-EPMC3384527</accession><cross_references><pubmed>17309277</pubmed><doi>10.1021/ol0701971 </doi></cross_references></HashMap>