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Abstract Oxidation of tertiary alcohol of the type 3-hydroxy-3-phenacyloxindoles using the combination of phenyliodine diacetate and molecular iodine in methanol results in oxidative cleavage of C2-C3 bond to form isocyanate… Click to show full abstract
Abstract Oxidation of tertiary alcohol of the type 3-hydroxy-3-phenacyloxindoles using the combination of phenyliodine diacetate and molecular iodine in methanol results in oxidative cleavage of C2-C3 bond to form isocyanate as an intermediate with its subsequent trapping by methanol to form ortho-carbamates of 1,3-diaryl carbonyl compounds which further undergoes concurrent cyclization to furnish 2-hydroxy-2-aryl/alkyl-2,3-dihydroquinolin-4(1H)-ones derivatives in good yields.
Keywords:
diacetate molecular;
phenyliodine diacetate;
hydroxy;
phenacyloxindoles using;
hydroxy phenacyloxindoles;
molecular iodine
Journal Title: Tetrahedron Letters
Year Published: 2020
Link to full text (if available)
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Journal Title: Tetrahedron Letters
Year Published: 2020
Link to full text (if available)
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recommendations!