<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>39</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>15</volume><submitter>Wang Y</submitter><pubmed_abstract>(-)-Isoguaiene was prepared from (&lt;i>S&lt;/i>)-citronellal in only 9-10 steps with good overall yields. Either a trienyne or a dienediyne metathesis and highly diastereoselective organocatalytic Michael additions of aldehydes derived from (&lt;i>S&lt;/i>)-citronellal served as the key transformations.</pubmed_abstract><journal>Beilstein journal of organic chemistry</journal><pagination>858-862</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6466796</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>An efficient synthesis of the guaiane sesquiterpene (-)-isoguaiene by domino metathesis.</pubmed_title><pmcid>PMC6466796</pmcid><pubmed_authors>Metz P</pubmed_authors><pubmed_authors>Darweesh AF</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Zimdars P</pubmed_authors><view_count>39</view_count></additional><is_claimable>false</is_claimable><name>An efficient synthesis of the guaiane sesquiterpene (-)-isoguaiene by domino metathesis.</name><description>(-)-Isoguaiene was prepared from (&lt;i>S&lt;/i>)-citronellal in only 9-10 steps with good overall yields. Either a trienyne or a dienediyne metathesis and highly diastereoselective organocatalytic Michael additions of aldehydes derived from (&lt;i>S&lt;/i>)-citronellal served as the key transformations.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019</publication><modification>2024-02-15T10:32:53.266Z</modification><creation>2019-06-06T22:56:20Z</creation></dates><accession>S-EPMC6466796</accession><cross_references><pubmed>31019578</pubmed><doi>10.3762/bjoc.15.83</doi></cross_references></HashMap>