Journal of Heterocyclic Chemistry · 1991 · 24 citations · 9 references
Natural SciencesChemistryMedicinal ChemistryDrug DiscoveryOrganic ChemistrySynthetic Medicinal ChemistryHeterocycle SynthesisHeterocyclic ChemistryOrganic SynthesisHeterocycle FunctionalizationNucleophilic ReactivityPyrazine ChemistryPyrazole ChemistryQuinoline ChemistryQuinoline SynthesisQuinoxaline ChemistryQuinoxaline Synthesis
Abstract Pyrazines and quinoxalines bearing 2‐substituents that direct ortho metalation reacted with lithium 2,2,6,6‐tetramethylpiperidide to produce 2‐substituted‐3‐lithiopyrazines and quinoxalines. These lithio reagents reacted with N ‐methoxy‐ N ‐methylbenzamide to give good to moderate yields of 3‐substituted pyrazinyl or quinoxalinylphenylmethanones. The 3‐methylthio substituents of some ketone products were oxidized to methylsulfonyl groups that were susceptible to nucleophilic displacement.
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N-methoxy-n-methylamides as effective acylating agents
Steven Nahm, Steven M. Weinreb · Tetrahedron Letters · 1981 · 1.8K citations
C. David Jones, Mark A. Winter, Kenneth S. Hirsch et al. · Journal of Medicinal Chemistry · 1990 · 70 citations · Full text