Reaction of arylpropargyl aldehydes with 2,3-bis-hydroxylamino-2,3-dimethylbutane: Synthesis of 2-(1-hydroxy-4,4,5,5-tetramethylimidazolidin-2-ylidene)-1-arylethanones Full article
Journal |
Tetrahedron
ISSN: 0040-4020 |
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Output data | Year: 2000, Volume: 56, Number: 51, Pages: 10075-10080 Pages count : DOI: 10.1016/S0040-4020(00)00978-9 | ||||||
Tags | hydroxylamine derivatives; propargyl aldehydes; 1-hydroxyimidazolidin-2-ylidenes | ||||||
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Abstract:
Reaction of arylpropargyl aldehydes with 2,3-dihydroxylamino-2,3-dimethylbutane results in the formation of 2-(1-hydroxy-4,4,5,5-tetramethylimidazolidin-2-ylidene)-1-arylethanones in high yields (70-80%). Allowing availability of propargyl aldehydes, this method gives new possibilities for the preparation of 2-(1-hydroxy-4,4,5,5-tetramethylimidazolidin-2-ylidene)-1-arylethanones. (C) 2000 Elsevier Science Ltd. All rights reserved.
Cite:
Tretyakov E.
, Tkachev A.
, Rybalova T.
, Gatilov Y.
, Knight D.
, Vasilevsky S.
Reaction of arylpropargyl aldehydes with 2,3-bis-hydroxylamino-2,3-dimethylbutane: Synthesis of 2-(1-hydroxy-4,4,5,5-tetramethylimidazolidin-2-ylidene)-1-arylethanones
Tetrahedron. 2000. V.56. N51. P.10075-10080. DOI: 10.1016/S0040-4020(00)00978-9 WOS Scopus РИНЦ
Reaction of arylpropargyl aldehydes with 2,3-bis-hydroxylamino-2,3-dimethylbutane: Synthesis of 2-(1-hydroxy-4,4,5,5-tetramethylimidazolidin-2-ylidene)-1-arylethanones
Tetrahedron. 2000. V.56. N51. P.10075-10080. DOI: 10.1016/S0040-4020(00)00978-9 WOS Scopus РИНЦ
Dates:
Published print: | Dec 1, 2000 |
Identifiers:
Web of science | WOS:000165736600025 |
Scopus | 2-s2.0-0034670508 |
Elibrary | 13340835 |
OpenAlex | W2953213384 |