<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Weber M</submitter><funding>NIGMS NIH HHS</funding><pagination>3600-3603</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4445844</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>56(23)</volume><pubmed_abstract>A possible biosynthetic link between atropurpuran, the hetidine diterpenoid alkaloids and the alkaloid arcutine and congeners is proposed. The feasibility of aspects of this biosynthesis, especially key 1,2-rearrangements, have been examined computationally.</pubmed_abstract><journal>Tetrahedron letters</journal><pubmed_title>Atropurpuran - Missing Biosynthetic Link Leading to the Hetidine and Arcutine C&lt;sub>20&lt;/sub>-Diterpenoid Alkaloids or an Oxidative Degradation Product?</pubmed_title><pmcid>PMC4445844</pmcid><funding_grant_id>R01 GM084906</funding_grant_id><pubmed_authors>Weber M</pubmed_authors><pubmed_authors>Owens K</pubmed_authors><pubmed_authors>Sarpong R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Atropurpuran - Missing Biosynthetic Link Leading to the Hetidine and Arcutine C&lt;sub>20&lt;/sub>-Diterpenoid Alkaloids or an Oxidative Degradation Product?</name><description>A possible biosynthetic link between atropurpuran, the hetidine diterpenoid alkaloids and the alkaloid arcutine and congeners is proposed. The feasibility of aspects of this biosynthesis, especially key 1,2-rearrangements, have been examined computationally.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Jun</publication><modification>2025-04-18T17:30:41.882Z</modification><creation>2019-03-27T01:52:14Z</creation></dates><accession>S-EPMC4445844</accession><cross_references><pubmed>26028789</pubmed><doi>10.1016/j.tetlet.2015.01.111</doi></cross_references></HashMap>