Synthesis of 3-nitro-5-acylpyridines by condensation of sodium nitromalonaldehyde/tosyl chloride with 2-amino-1-acyl olefins. Evidence for the intermediacy of 3-chloro-2-nitroacrolein

Synthesis of 3-nitro-5-acylpyridines by condensation of sodium nitromalonaldehyde/tosyl chloride with 2-amino-1-acyl olefins. Evidence for the intermediacy of 3-chloro-2-nitroacrolein

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Veröffentlicht in:Journal of organic chemistry 1984, Vol.49 (1), p.193-195
Hauptverfasser: HOFFMAN, J. M, PHILLIPS, B. T, COCHRAN, D. W
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Sprache:eng
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Chemistry
Exact sciences and technology
Heterocyclic compounds
Heterocyclic compounds with only one n hetero atom and condensed derivatives
Organic chemistry
Preparations and properties
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container_title Journal of organic chemistry
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creator HOFFMAN, J. M
PHILLIPS, B. T
COCHRAN, D. W
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subjects Chemistry
Exact sciences and technology
Heterocyclic compounds
Heterocyclic compounds with only one n hetero atom and condensed derivatives
Organic chemistry
Preparations and properties
title Synthesis of 3-nitro-5-acylpyridines by condensation of sodium nitromalonaldehyde/tosyl chloride with 2-amino-1-acyl olefins. Evidence for the intermediacy of 3-chloro-2-nitroacrolein
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