2015
DOI: 10.3762/bjoc.11.226
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Copper-mediated synthesis of N-alkenyl-α,β-unsaturated nitrones and their conversion to tri- and tetrasubstituted pyridines

Abstract: SummaryA Chan–Lam reaction has been used to prepare N-alkenyl-α,β-unsaturated nitrones, which undergo a subsequent thermal rearrangement to the corresponding tri- and tetrasubstituted pyridines. The optimization and scope of these transformations is discussed. Initial mechanistic experiments suggest a reaction pathway involving oxygen transfer followed by cyclization.

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Cited by 33 publications
(14 citation statements)
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“…However, using cyclic N ‐vinyl nitrones failed to afford the desired products at 60 °C, resulting in only decomposition of the starting materials. Lowering the temperature allowed the successful reaction of cyclic N ‐vinyl nitrones ( 1 r – t ), which afforded the desired products 3 r – t in good yields, incorporating six‐ and seven‐membered rings accompanied by some pyridine byproducts also reported by Anderson's group . Interestingly, compound 3 s was obtained in 59% yield as only one isomer, even though a phenyl group was present on the six‐membered ring.…”
Section: Methodsmentioning
confidence: 75%
“…However, using cyclic N ‐vinyl nitrones failed to afford the desired products at 60 °C, resulting in only decomposition of the starting materials. Lowering the temperature allowed the successful reaction of cyclic N ‐vinyl nitrones ( 1 r – t ), which afforded the desired products 3 r – t in good yields, incorporating six‐ and seven‐membered rings accompanied by some pyridine byproducts also reported by Anderson's group . Interestingly, compound 3 s was obtained in 59% yield as only one isomer, even though a phenyl group was present on the six‐membered ring.…”
Section: Methodsmentioning
confidence: 75%
“…Good yields were achieved, and the Eisomers were obtained as the major products (Scheme 62). 48 The reaction proceeded smoothly for electron-donating-and electron-withdrawing-substituted α,β-unsaturated oximes, as well as heteroarene-substituted α,β-unsaturated oximes. Interestingly, when cyclooctadiene was added to the reaction mixture, the amount of copper acetate could be reduced to 10 mol%.…”
Section: Scheme 61 Cu-mediated Direct N-vinylation Reactionmentioning
confidence: 97%
“…N-Vinylnitrones have been prepared from fluorenone oxime by the Cu(OAc) 2 -mediated reactions with alkenylboronic acids (eq 25). 98,99 Similarly, Cu(OAc) 2promoted reactions of malonate-derived oximes with vinylboronic acids give N-alkenylnitrones, which undergo 4πelectrocyclization to form azetidine nitrones (Scheme 5). 100 Copper-catalyzed reaction of oximes with cyclopropenes using chiral phosphines gives chiral N-cyclopropylnitrones (eq 26).…”
Section: Reaction Of Oximesmentioning
confidence: 99%