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Gallium-Mediated Allyl Transfer from Bulky Homoallylic Alcohol to Aldehydes via Retro-allylation: Stereoselective Synthesis of Both <i>e</i><i>rythro</i>- and <i>t</i><i>hreo</i>-Homoallylic Alcohols<sup>1</sup>
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Citations
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References
2005
Year
-Crotylgallium ReagentsCross-coupling ReactionEngineeringAlkene MetathesisBulky Homoallylic AlcoholOrganic ChemistryCatalysisGallium-mediated Allyl TransferChemistryStereoselective SynthesisBulky Gallium HomoallylicThreo-homoallylic AlcoholsEnantioselective SynthesisBiomolecular Engineering
Retro-allylation of bulky gallium homoallylic alkoxides occurs to generate (Z)- and (E)-crotylgallium reagents stereospecifically, starting from erythro- and threo-homoallylic alcohols, respectively. The (Z)- and (E)-crotylgallium reagents immediately reacted with aromatic aldehydes to afford the corresponding erythro- and threo-homoallylic alcohols, respectively. [reaction: see text]
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