In:
Zeitschrift für Naturforschung B, Walter de Gruyter GmbH, Vol. 56, No. 10 ( 2001-10-1), p. 1074-1078
Abstract:
Enaminones react with a variety of active methyl and methylene reagents in presence of ammonium acetate to yield functionally substituted pyridines in good yields. The reaction proceeded via initial Michael addition across the double bond followed by cyclization. The reaction of enaminone with aromatic aldehyde in acetic acid/ammonium acetate afforded the dihydropyridine that was oxidized to the corresponding pyridine.
Type of Medium:
Online Resource
ISSN:
1865-7117
,
0932-0776
DOI:
10.1515/znb-2001-1016
Language:
English
Publisher:
Walter de Gruyter GmbH
Publication Date:
2001
detail.hit.zdb_id:
2078109-X
detail.hit.zdb_id:
124635-5
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