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0033020763
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For reviews, see: (a) Ahlbrecht H., Beyer U. Synthesis. 1999;365-390 (b) Katrizky A.R., Piffl M., Lang H., Anders E. Chem. Rev. 99:1999;665-722 (c) Crimmins M.T., Nantermet P.G. Org. Prep. Proced. 25:1993;41-81 (d) Kuwajima I., Nakamura E. Top. Curr. Chem. 155:1990;1-39 (e) Stowell J.C. Chem. Rev. 84:1984;409-436 (f) Werstiuk N.H. Tetrahedron. 39:1983;205-268.
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For reviews, see: (a) Ahlbrecht H., Beyer U. Synthesis. 1999;365-390 (b) Katrizky A.R., Piffl M., Lang H., Anders E. Chem. Rev. 99:1999;665-722 (c) Crimmins M.T., Nantermet P.G. Org. Prep. Proced. 25:1993;41-81 (d) Kuwajima I., Nakamura E. Top. Curr. Chem. 155:1990;1-39 (e) Stowell J.C. Chem. Rev. 84:1984;409-436 (f) Werstiuk N.H. Tetrahedron. 39:1983;205-268.
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For reviews, see: (a) Ahlbrecht H., Beyer U. Synthesis. 1999;365-390 (b) Katrizky A.R., Piffl M., Lang H., Anders E. Chem. Rev. 99:1999;665-722 (c) Crimmins M.T., Nantermet P.G. Org. Prep. Proced. 25:1993;41-81 (d) Kuwajima I., Nakamura E. Top. Curr. Chem. 155:1990;1-39 (e) Stowell J.C. Chem. Rev. 84:1984;409-436 (f) Werstiuk N.H. Tetrahedron. 39:1983;205-268.
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For reviews, see: (a) Ahlbrecht H., Beyer U. Synthesis. 1999;365-390 (b) Katrizky A.R., Piffl M., Lang H., Anders E. Chem. Rev. 99:1999;665-722 (c) Crimmins M.T., Nantermet P.G. Org. Prep. Proced. 25:1993;41-81 (d) Kuwajima I., Nakamura E. Top. Curr. Chem. 155:1990;1-39 (e) Stowell J.C. Chem. Rev. 84:1984;409-436 (f) Werstiuk N.H. Tetrahedron. 39:1983;205-268.
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For reviews, see: (a) Ahlbrecht H., Beyer U. Synthesis. 1999;365-390 (b) Katrizky A.R., Piffl M., Lang H., Anders E. Chem. Rev. 99:1999;665-722 (c) Crimmins M.T., Nantermet P.G. Org. Prep. Proced. 25:1993;41-81 (d) Kuwajima I., Nakamura E. Top. Curr. Chem. 155:1990;1-39 (e) Stowell J.C. Chem. Rev. 84:1984;409-436 (f) Werstiuk N.H. Tetrahedron. 39:1983;205-268.
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85031219025
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7 and (bis-dimethylamido) phosphoryl chloride gave a mixture of 4 and the transposed product 5 (E=H) in poor yield (50%)
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7 and (bis-dimethylamido) phosphoryl chloride gave a mixture of 4 and the transposed product 5 (E=H) in poor yield (50%).
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31
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85031216073
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The change of a bis-dimethylamine group by an ethoxy group, or, a fortiori, the replacement of the two bis-dimethylamine groups by two ethoxy groups at phosphorus into 4, led to phosphoramides that were not deprotonated by n-BuLi
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The change of a bis-dimethylamine group by an ethoxy group, or, a fortiori, the replacement of the two bis-dimethylamine groups by two ethoxy groups at phosphorus into 4, led to phosphoramides that were not deprotonated by n-BuLi.
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35
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0001026160
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