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For examples of cross coupling reactions involving α-halo enol ethers: (a) R.W. Friesen, R.W. Loo, and C.F. Sturino. Can. J. Chem. 72, 1262 (1994);
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9
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For preparation of a-halo enol ethers using strong bases: a
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For preparation of a-halo enol ethers using strong bases: (a) E. Boyd, M.R. Hallett, R.V.H. Jones, J.E. Painter, P. Patel, P. Quayle, and A.J. Waring. Tetrahedron Lett. 47, 8337 (2006);
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(c) S.F. Martin. Pure Appl. Chem. 75, 63 (2003). For preparation of α-halo enol ethers via stannyl intermediates:
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Y. Amiel. In The chemistry of functional groups. Supplement C, The chemistry of triple bonded functional groups. Part I. Edited by S. Patai and Z. Rappoport. Wiley, Chichester. 1983. pp. 345-347;
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(e) Y. Amiel. In The chemistry of functional groups. Supplement C, The chemistry of triple bonded functional groups. Part I. Edited by S. Patai and Z. Rappoport. Wiley, Chichester. 1983. pp. 345-347;
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Radical 4 is expected to interconvert very slowly since it is known that a-oxy vinyl radicals possess a very high energy barrier to rotation; see: (a) J.A. Kampmeier, M.S. Liu, S. Soloway, and D.K. Wedegaertner. J. Am. Chem. Soc. 93, 3809 (1971);
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Radical 4 is expected to interconvert very slowly since it is known that a-oxy vinyl radicals possess a very high energy barrier to rotation; see: (a) J.A. Kampmeier, M.S. Liu, S. Soloway, and D.K. Wedegaertner. J. Am. Chem. Soc. 93, 3809 (1971);
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For other methods for preparing β,β-dialkylated α-iodo enol ethers, see: a
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For other methods for preparing β,β-dialkylated α-iodo enol ethers, see: (a) H.R. Sonawane, B.S. Nanjundiah, and M.D. Panse. Tetrahedron Lett. 26, 3507 (1985);
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