Publication | Closed Access
Ring‐Opening of 5‐(Bromomethyl)‐2‐isoxazolines to β,γ‐Enoximes—A New Principle for the γ‐Substitution of Allyl Bromides by α‐Functionalized Alkyl Groups
23
Citations
8
References
1979
Year
Secondary ProductsCross-coupling ReactionEnantioselective SynthesisEngineeringAllyl BromidesBiochemistryNatural SciencesNew PrincipleOrganic ChemistryStereoselective SynthesisChemistryHeterocycle Chemistryα‐Functionalized Alkyl GroupsControlled γ-SubstitutionBiomolecular Engineering
Reductive-eliminating ring opening of isoxazolines (2) is the key step of a reaction sequence for controlled γ-substitution of allyl bromides (1). The reaction may give oximes (3), ketones (4), or their secondary products.
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