Regioselective acylation of benzoselenazolinone

Article abstract of DOI:10.1080/00397919308009820

Substitutions on benzoselenazolinone were performed by using successively (i) aliphatic or aromatic acids and (ii) acid chlorides in the presence of (i) polyphosphoric acid and (ii) aluminium chloride in dimethylformamide. Regioselective acylation at C₆ position was demonstrated by ¹H NMR using Nuclear Overhauser Effect.

Full text of DOI:10.1080/00397919308009820

Synthetic Communications
ISSN: 0039-7911 (Print) 1532-2432 (Online) Journal homepage: http://www.tandfonline.com/loi/lsyc20
Regioselective Acylation of Benzoselenazolinone
V. Galet , M. P. Vaccher , J. L. Bernier , J. P. Henichart & D. Lesieur
To cite this article: V. Galet , M. P. Vaccher , J. L. Bernier , J. P. Henichart & D. Lesieur (1993)
Regioselective Acylation of Benzoselenazolinone, Synthetic Communications, 23:5, 621-629,
DOI: 10.1080/00397919308009820
To link to this article: http://dx.doi.org/10.1080/00397919308009820
Published online: 27 Oct 2006.
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Date: 21 September 2015, At: 08:15