Publication | Closed Access
Regioselective functionalization of 2-arylazetidines: evaluating the ortho-directing ability of the azetidinyl ring and the α-directing ability of the N-substituent
42
Citations
25
References
2013
Year
Azetidinyl RingRegioselectivity SwitchRegioselective Lithiation-functionalizationBiochemistryEngineeringNatural SciencesDiversity-oriented SynthesisRegioselective FunctionalizationOrtho-directing AbilityOrganic ChemistryStereoselective SynthesisChemistryα-Benzylic LithiationSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
The regioselective lithiation-functionalization of 2-arylazetidines has been explored. The nature of the N-substituent is mainly responsible for a regioselectivity switch. ortho-Lithiation occurred, using hexyllithium as a greener base, in N-alkylazetidines, while α-benzylic lithiation has been observed with N-Boc azetidines.
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