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THE WITTIG REACTION WITH 2,2-DIMETHYL-l,3-INDANDIONE

Year 1988, Volume: 34 Issue: 01.02, 48 - 52, 01.01.1899
https://doi.org/10.1501/Commub_0000000486

Abstract

The reactions of 2,2-dimethyl-l,3-indandione (I) with several Wittig reagents have been studied. When I was reacted with one or two equimolar amounts of active phosphoranes, such as methylene and ethylidenetriphenylphosphorane, bismethylene- and bisethylidene deriva- tives of the indandione were obtained in fairly good yields. The reactions of I with resonance- stabilized phosphoranes such as ethoxycarbony!methylene-2—butylidene— and carboethoxy— 2-methyl-2-propylidenetriphenylphosphorane gave monoalkylideneindanones in moderate or in pocr yields at severe conditions. On the contrary, the reaction of I with carboethoxymethyle- netriphenylphosphorane in sealed tube gave the bisalkylidene derivative of the indandione at 160°C.

References

  • Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
Year 1988, Volume: 34 Issue: 01.02, 48 - 52, 01.01.1899
https://doi.org/10.1501/Commub_0000000486

Abstract

References

  • Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
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Details

Primary Language English
Subjects Chemical Engineering
Journal Section Research Article
Authors

Tahsin Uyar This is me

Publication Date January 1, 1899
Published in Issue Year 1988 Volume: 34 Issue: 01.02

Cite

Vancouver Uyar T. THE WITTIG REACTION WITH 2,2-DIMETHYL-l,3-INDANDIONE. Commun. Fac. Sci. Univ. Ank. Ser. B. 1899;34(01.02):48-52.

Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering

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