Five-Membered 2,3-Dioxo Heterocycles: XLVI. Reaction of 5-Aryl-4-quinoxalinyl-2,3-dihydrofuran-2,3-diones with Aldehydes and Ketones. Molecular and Crystalline Structure of 5-(3-p-Tolylquinoxalin-2-yl)-4H-1,3-dioxine- 2-spiro-2'-adamantan-4-one View Full Text


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Article Info

DATE

2004-07

AUTHORS

N. Yu. Lisovenko, A. N. Maslivets, Z. G. Aliev

ABSTRACT

Aroyl(quinoxalinyl)ketenes generated by thermolysis of 5-aryl-4-(3-arylquinoxalin-2-yl)-2,3-di-hydrofuran-2,3-diones act as dienes in [4 + 2]-cycloaddition at the carbonyl group of aldehydes and ketones to afford 2-substituted 6-aryl-5-(3-arylquinoxalin-2-yl)-4H-1,3-dioxin-4-ones. The structure of 5-(3-p-tolylquino-xalin-2-yl)-4H-1,3-dioxine-2-spiro-2'-adamantan-4-one was proved by X-ray analysis.

PAGES

1053-1057

Identifiers

URI

http://scigraph.springernature.com/pub.10.1023/b:rujo.0000045203.69639.83

DOI

http://dx.doi.org/10.1023/b:rujo.0000045203.69639.83

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1051500078


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