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Merck
CN

Conversion of indanone oximes into isocarbostyrils.

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

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.

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Sigma-Aldrich
异喹诺酮, 98%