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Merck

Conversion of indanone oximes into isocarbostyrils.

Bioorganic & medicinal chemistry letters (2006-10-27)
Yasuhiro Torisawa, Shinji Aki, Jun-ichi Minamikawa
ZUSAMMENFASSUNG

New and effective method for the Beckmann rearrangement of indanone oxime mesylate is described, in which a selective and controlled production of the isomeric isocarbostyrils is achieved.

MATERIALIEN
Produktnummer
Marke
Produktbeschreibung

Sigma-Aldrich
Methansulfonylchlorid, ≥99.7%
Sigma-Aldrich
Methansulfonylchlorid, purum, ≥98.0% (AT)
Sigma-Aldrich
1-Isochinolinol, 98%