68981-78-2Relevant articles and documents
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Giam,C.S.,Hauck,A.E.
, p. 615 - 616 (1978)
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SOLVENT AND TEMPERATURE EFFECTS ON THE NUCLEOPHILIC ADDITION OF ORGANOLITHIUMS TO 3-(4,4-DIMETHYLOXAZOLIN-2-YL)PYRIDINE. SYNTHESIS OF STABILIZED 1,2-, 1,4- AND/OR 1,6-DIHYDROPYRIDINES
Dubey, Sushil K.,Knaus, Edward E.
, p. 125 - 134 (2007/10/02)
The reaction of 3-(4,4-dimethyloxazolin-2-yl)pyridine (1) with nucleophilic organolithium reagents afforded stabilized N-unsubstituted 1,2-, 1,4- and/or 1,6-dihydropyridines.Reaction of 1 with phenyllithium gave a mixture of 1,2- (2) and 1,4-dihydropyridi
Substitutions on Pyridines Activated by Oxazolines via Nucleophilic Additions or Metalation-Alkylation
Meyers, A. I.,Gabel, Richard A.
, p. 2633 - 2637 (2007/10/02)
Pyridyloxazolines, derived from nicotinic acid or isonicotinic acid, have been shown to metalate at the 4- and 3-positions, respectively.These react with a variety of electrophiles to provide 4- and 3-substituted pyridines in good yield.Alternatively, 3-pyridyloxazolines, when treated with organolithium or Grignard reagents, give addition to the 4-position and provide a series of 4-substituted 1,4-dihydropyridines.