Metal-free annulation of β-acylamino ketones: facile access to spirooxazolines and oxazolines via oxidative C–O bond formation

TitleMetal-free annulation of β-acylamino ketones: facile access to spirooxazolines and oxazolines via oxidative C–O bond formation
Publication TypeJournal Article
Year of Publication2018
AuthorsChavan, SS, Rupanawar, BD, Kamble, RB, Shelke, AM, Suryavanshi, G
JournalOrganic Chemistry Frontiers
Volume5
Issue4
Pagination544-548
Date PublishedOCT
AbstractA metal-free annulation reaction of β-acylamino ketone derivatives has been reported for the synthesis of a group of functionalized spirooxazolines and oxazolines in good to excellent yields. The reaction proceeds via phenyliodine(III) diacetate (PIDA)-mediated oxidative C–O bond formation in the presence of BF3–OEt2. The mild reaction conditions, broad substrate scope, simple execution and synthetic potential of the products make this novel protocol very attractive.
DOI10.1039/C7QO00783C
Type of Journal (Indian or Foreign)Foreign
Impact Factor (IF)4.955
Divison category: 
Chemical Engineering & Process Development

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