Publication | Closed Access
Access to Pyrrolo- and Pyrido[1,2-<i>a</i>]indole Derivatives by Intramolecular Nitrone Cycloadditions. Effect of Steric Factors on the Regioselective Product Formation
38
Citations
15
References
2000
Year
Intramolecular Nitrone CycloadditionsEngineeringHeterocyclicSteric FactorsOrganic ChemistryN-allyl-substituted 2-IndolecarbaldehydesStereoselective SynthesisChemistryHeterocycle ChemistryEnantiopure FormRegioselective Product FormationSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
On starting from N-allyl-substituted 2-indolecarbaldehydes and exploiting the intramolecular nitrone cycloaddition methodology, we synthesized a number of the title fused-ring indole derivatives in racemic as well as enantiopure form.
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