Sterically hindered 3-thienylidene-4-piperidones Full article
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Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science
ISSN: 2376-8444 , E-ISSN: 0568-5230 |
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Output data | Year: 1986, Volume: 35, Number: 12, Pages: 2511-2516 Pages count : 6 DOI: 10.1007/bf01474210 | ||||
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Abstract:
1. Condensation of triacetoneamine with thiophene aldehyde and its derivatives in the presence of base gave 3-mono and 3,5-bis-thienylidene-2,2,6,6-tetramethyl-4-piperidones. 2. 2,2,6,6-Tetramethyl-3 (2-thienylidene)-4-piperidone did not add butyl lithium at the carbonyl group but was metallated at the 5-position of the thiophene ring. In the case of reaction of 2,2,6,6-tetramethyl-5 (2-thienylidene)-piperidine-3,5-dione with butyl lithium both metallation and 1,4-addition at the conjugated C=O group were observed.
Cite:
Myshkina L.A.
, Stoyanovich F.M.
, Gol'dfarb Y.L.
, Kazarina E.K.
Sterically hindered 3-thienylidene-4-piperidones
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science. 1986. V.35. N12. P.2511-2516. DOI: 10.1007/bf01474210 OpenAlex
Sterically hindered 3-thienylidene-4-piperidones
Bulletin of the Academy of Sciences of the USSR, Division of Chemical Science. 1986. V.35. N12. P.2511-2516. DOI: 10.1007/bf01474210 OpenAlex
Identifiers:
OpenAlex: | W2095077351 |
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