Trithia- and dithiaselenapentalenes from benzylidene-1,2-dithioles and heterocumulenes
โ Scribed by Yunxiang Ding; Jie Kong; David H. Reid
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 244 KB
- Volume
- 8
- Category
- Article
- ISSN
- 1042-7163
No coin nor oath required. For personal study only.
โฆ Synopsis
Deprotonation of the 5-aryl-3-benzyl-1k 4 ,2-dithiol-1ylium iodides (6a-6d) obtained by reaction of the 1aryl-4-phenylbutan-1,3-diones (5a-5d) with hydrogen sulfide and iodine in ethanol gave the stable 5-aryl-3benzylidene-3H-1,2-dithioles (3a-3d), respectively. The dithioles (3a-3d) underwent thermal cycloaddition reactions with isoselenocyanates and isothiocyanates to give the 2-(substituted amino)-5-aryl-3phenyl-6,6ak 4 -dithia-1-selenapentalenes (7a-7h) and the 2-(substituted amino)-5-aryl-3-phenyl-1,6,6ak 4trithiapentalenes (8a-8l), respectively. The dithioles (3a-3d) reacted with isocyanates to give the N-substituted-2-phenyl-2-(5-aryl-3H-1,2-dithiol-3-ylidene) acetamides (11a-11h). แญง 1997
๐ SIMILAR VOLUMES
1,6ak 4 -Dithia-6-azapentalenes (7a)-( 7h), (12a), and (12b) have been synthesized by the reaction of 5-aryl-3-benzylidene-3H-1,2-dithioles with isonitriles in the presence of phosphoryl chloride and by the reaction of 3-benzyl-and 3-methyl-1k 4 , 2-dithiol-1-ylium salts with isonitriles. Possible m