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Water mediated procedure for preparation of stereoselective oximes as inhibitors of MRCK kinase

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Abstract Stereoselective aldoximes, preferably Z form have been obtained from α-cyano substituted carbonyl conjugated alkenes. This reaction occurs through Michael addition type reaction followed by retro-Knoevenagel reaction without transition-metal catalysis… Click to show full abstract

Abstract Stereoselective aldoximes, preferably Z form have been obtained from α-cyano substituted carbonyl conjugated alkenes. This reaction occurs through Michael addition type reaction followed by retro-Knoevenagel reaction without transition-metal catalysis via C–C bond cleavage. These oximes are evaluated against cancer cell lines employing mechanistic study. Two oximes showed significant cytotoxic activity, which through in silico studies were found to inhibit MRCK Kinase, responsible for metastatic spread of cancer mortality.

Keywords: stereoselective oximes; preparation stereoselective; mediated procedure; water mediated; mrck kinase; procedure preparation

Journal Title: Journal of Molecular Structure
Year Published: 2020

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