CYCLOCONDENSATION OF N-(2-BROMOETHYL)PHTHALIMIDE WITH THE DIANION OF ISOBUTYRIC ACID TO A FUNCTIONALIZED 2,3-DIHYDROOXAZOLO[2,3]ISOINDOL-5(9BH)-ONE DERIVATIVE

Authors
DEKIMPE N VIRAG M KEPPENS M SCHEINMANN F STACHULSKI AV
Citation
N. Dekimpe et al., CYCLOCONDENSATION OF N-(2-BROMOETHYL)PHTHALIMIDE WITH THE DIANION OF ISOBUTYRIC ACID TO A FUNCTIONALIZED 2,3-DIHYDROOXAZOLO[2,3]ISOINDOL-5(9BH)-ONE DERIVATIVE, Journal of chemical research. Synopses, (6), 1995, pp. 252-253
Citations number
8
Categorie Soggetti
Chemistry
Journal title
Journal of chemical research. Synopses → ACNP
ISSN journal
03082342
Issue
6
Year of publication
1995
Pages
252 - 253
Database
ISI
SICI code
0308-2342(1995):6<252:CONWTD>2.0.ZU;2-V
Abstract
Contrary to a previous report describing that the condensation or N-(2 -bromoethyl)phthalimide with the dianion of isobutyric acid affords -1 -yl)carbonyl]phenyl}-2,2-dimethyl-3-oxopropanoic acid, we report that this reaction in fact leads to drooxazolo[2,3-a]isoindol-9b-yl)-2-meth ylpropanoic acid.