<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>90(11)</volume><submitter>Lipshutz BH</submitter><pubmed_abstract>The two laboratory reactions focus on teaching several concepts associated with green chemistry. Each uses a commercial, nontoxic, and biodegradable surfactant, TPGS-750-M, to promote organic reactions within the lipophilic cores of nanoscale micelles in water. These experiments are based on work by K. Barry Sharpless (an azide-alkyne "click" reaction) and Robert Grubbs (an olefin cross-metathesis reaction); both are suitable for an undergraduate organic laboratory. The copper-catalyzed azide-alkyne [3+2] cycloaddition of benzyl azide and 4-tolylacetylene is very rapid: the triazole product is readily isolated by filtration and is characterized by thin-layer chromatography and melting point analysis. The ruthenium-catalyzed olefin cross-metathesis reaction of benzyl acrylate with 1-hexene </pubmed_abstract><journal>Journal of chemical education</journal><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3855046</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>"Click" and Olefin Metathesis Chemistry in Water at Room Temperature Enabled by Biodegradable Micelles.</pubmed_title><pmcid>PMC3855046</pmcid><pubmed_authors>Wenzel AG</pubmed_authors><pubmed_authors>Vosburg DA</pubmed_authors><pubmed_authors>Lipshutz BH</pubmed_authors><pubmed_authors>Davis VK</pubmed_authors><pubmed_authors>Boskovic Z</pubmed_authors><pubmed_authors>Crowe CS</pubmed_authors><pubmed_authors>Whittemore HC</pubmed_authors></additional><is_claimable>false</is_claimable><name>"Click" and Olefin Metathesis Chemistry in Water at Room Temperature Enabled by Biodegradable Micelles.</name><description>The two laboratory reactions focus on teaching several concepts associated with green chemistry. Each uses a commercial, nontoxic, and biodegradable surfactant, TPGS-750-M, to promote organic reactions within the lipophilic cores of nanoscale micelles in water. These experiments are based on work by K. Barry Sharpless (an azide-alkyne "click" reaction) and Robert Grubbs (an olefin cross-metathesis reaction); both are suitable for an undergraduate organic laboratory. The copper-catalyzed azide-alkyne [3+2] cycloaddition of benzyl azide and 4-tolylacetylene is very rapid: the triazole product is readily isolated by filtration and is characterized by thin-layer chromatography and melting point analysis. The ruthenium-catalyzed olefin cross-metathesis reaction of benzyl acrylate with 1-hexene </description><dates><release>2013-01-01T00:00:00Z</release><publication>2013 Nov</publication><modification>2025-04-04T12:47:22.108Z</modification><creation>2019-03-27T01:18:10Z</creation></dates><accession>S-EPMC3855046</accession><cross_references><pubmed>24324282</pubmed><doi>10.1021/ed300893u</doi></cross_references></HashMap>