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Benzimidazolinetriones. Reactions of 2,5,6‐ and 2,4,7‐benzimidazolinetriones
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Benzimidazolinetriones. Reactions of 2,5,6‐ and 2,4,7‐benzimidazolinetriones
作者:
Louis C. March,
Madeleine M. Joullié,
期刊:
Journal of Heterocyclic Chemistry
(WILEY Available online 1970)
卷期:
Volume 7,
issue 1
页码: 39-42
ISSN:0022-152X
年代: 1970
DOI:10.1002/jhet.5570070105
出版商: Wiley‐Blackwell
数据来源: WILEY
摘要:
AbstractThe condensation of 2,5,6‐benzimidazolinetrione with ethylenediamine resulted in the formation of the 1,3‐dihydro‐2H‐imidazo[4,5‐g]quinoxalin‐2‐one ring system. The reaction of this trione with excess ethanethiol resulted in the isolation of three hydroquinones which were oxidized to the respective quinones. 2,4,7‐Benzimidazolinetrione was shown to undergo a Diels‐Alder reaction with isoprene and a mono‐addition reactio
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