Regioselective acylation of benzoselenazolinone

DOI: 10.1080/00397919308009820

Source and publish data:

Synthetic Communications p. 621 - 629 (1993)

Update date:2022-09-26

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Authors:

Galet Galet

Vaccher Vaccher

Bernier Bernier

Henichart

Lesieur Lesieur

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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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