Journal
TETRAHEDRON
Volume 69, Issue 21, Pages 4353-4357Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2013.02.049
Keywords
2-Aminoindolizine; Pyrrole ring synthesis; CH-acids; 2-Chloro-Nethoxycarbonyl-methylpyridinium bromide
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Funding
- Russian Foundation of Basic Research (RFBR) [12-03-00644a]
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2-Chloro-N-ethoxycarbonylmethylpyridinium bromide reacts with substituted acetonitriles in two steps; the initially formed pyridine anhydro baseses undergo further ring closure to 2-amino-3-ethoxycarbonylindolizines. (C) 2013 Elsevier Ltd. All rights reserved.
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