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- W2912791423 endingPage "104" @default.
- W2912791423 startingPage "51" @default.
- W2912791423 abstract "This review summarizes the current status of the preparation of spiro-heterocycles fused with a pyranose or furanose carbohydrate skeleton, using free radical chemistry. A variety of heterospiro[m.n]alkane bicyclic structures (m = 3–5, n = 4–6) possessing one, two, or three heteroatoms (N, O, Si, S) have been collected, in addition to three different 1,6,8-trioxadispiro-tetradecane and 1,6,8-trioxadispiro-pentadecane tricyclic systems. C(sp3)–H bond functionalization by 1,5- or 1,6-hydrogen atom transfer (HAT) initiated by C(sp3)-, C(sp2)-, O-, or N-radicals and 5-exo-trig or 6-exo-trig cyclization reactions are the most useful strategies employed for the construction of the heterocyclic rings. The intramolecular HAT promoted by photoexcited monoketones, α-diketones, furanones, and succinimides via a Norrish type II–Yang cyclization process has also been successfully applied." @default.
- W2912791423 created "2019-02-21" @default.
- W2912791423 creator A5008874396 @default.
- W2912791423 creator A5032626084 @default.
- W2912791423 date "2019-01-01" @default.
- W2912791423 modified "2023-10-08" @default.
- W2912791423 title "Carbohydrate Spiro-heterocycles via Radical Chemistry" @default.
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