Back to Search Start Over

Carbanion Rearrangements. Collision-Induced Reactions of Enolate Negative Ions Derived From Dimethyl Succinates and Hexane-2,5-Dione

Authors :
Raftery, MJ
Raftery, MJ
Bowie, JH
Bowie, JH
Source :
Australian Journal of Chemistry; 1987, Vol. 40 Issue: 4 p711-721, 11p
Publication Year :
1987

Abstract

Enolate ion MeOCOCHCH2CO2Me fragments through the intermediacy of two ion complexes [ MeOCO (CH2=CHCO2Me)] and [ MeO-(O=C=CHCH2CO2Me)]. The major fragmentations produce CH2=C=C( OMe )O-+HCO2Me and O=C=CH- CH=C( OMe ). Similar ion complexes are formed from methyl-substituted succinates , but their fragmentations are often different from those outlined above: e.g. MeOCOC (Me)C(Me)2CO2Me - [ MeOCO (M2C=CmeCO2Me)] → CH2(Me)C=C(Me)CO2- Me+HCO2Me. The corresponding enolate from hexane-2,s-dione (MeCOCHCH2COMe) fragments through the acetyl anion complex [ MeCO (CH2=CHCO2Me)].

Details

Language :
English
ISSN :
00049425 and 14450038
Volume :
40
Issue :
4
Database :
Supplemental Index
Journal :
Australian Journal of Chemistry
Publication Type :
Periodical
Accession number :
ejs8411288
Full Text :
https://doi.org/10.1071/CH9870711