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A CONVENIENT SYNTHESIS OF CONSTITUTIONALLY DIVERSE N-HYDROXYPHENYLETHYL-ISOINDOLINONES
UNE TECHNIQUE SOUPLE ET EFFICACE D'ASSEMBLAGE D'UNE VARIETE DE N-HYDROXYPHENYLETHYL-ISOINDOLINONES


MAGALI LORION, ÉRIC DENIAU, AXEL COUTURE, PIERRE GRANDCLAUDON *
UNIVERSITÉ DES SCIENCES ET TECHNOLOGIES DE LILLE 1, UMR CNRS 8009 "CHIMIE ORGANIQUE ET MACROMOLÉCULAIRE", LABORATOIRE DE CHIMIE ORGANIQUE PHYSIQUE, BÂTIMENT C3(2), F-59655 VILLENEUVE D'ASCQ CEDEX, FRANCE

Issue:

SCSCC6, Volume X, No. 2

Section:

Volume X, No. 2 (2009)

Abstract:

A variety of polyalkoxylated N-hydroxyphenethyl-isoindolinones has been assembled by an anionic cyclization process applied to suitably substituted N-(ortho-bromobenzyl)-4-phenyloxazolidinone derivatives.

Keywords:

carbanion, oxazolidinones, ring opening, ring closure, lactams, bicyclic compounds, isoindolinones.

Code [ID]:

CSCC6200910V02S01A0003 [0002631]

Full paper:

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