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Recently, radical mediated C-P bond formations have been applied to the synthesis of (difluoromethylene)phosphonates: (a) Herpin, T. F.; Houlton, J. S.; Motherwell, W. B.; Roberts, B. P.; Weibel, J.-M. J. Chem. Soc., Chem. Commun. 1996, 613. (b) Piettre, S. R. Tetrahedron Lett. 1996, 37, 2233.
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Recently, radical mediated C-P bond formations have been applied to the synthesis of (difluoromethylene)phosphonates: (a) Herpin, T. F.; Houlton, J. S.; Motherwell, W. B.; Roberts, B. P.; Weibel, J.-M. J. Chem. Soc., Chem. Commun. 1996, 613. (b) Piettre, S. R. Tetrahedron Lett. 1996, 37, 2233.
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35
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0001186360
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The similar strategy have been applied to an efficient synthesis of (α,α-difluroallyl)carboxylates: Taguchi, T.; Kitagawa, O.; Morikawa, T.; Nishiwaki, T.; Uehara, H.; Endo, H.; Kobayashi, Y. Tetrahedron Lett. 1986, 27, 6103.
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36
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85033821688
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note
-
The loss of starting olefinic geometry might arise from nonstereospecific radical addition of 3 to phenylacetylene, a contamination product during the preparation of (Z)-β-bromostyrene.
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37
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85033813968
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note
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11,18
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-
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38
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85033809463
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note
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23 (Matrix Presented)
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-
-
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40
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49449125517
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Burton, D. J.; Flynn, R. M. J. Fluorine Chem. 1977, 10, 329. Mahmood, T.; Shreeve, J. M. Synth. Commun. 1987, 17, 71.
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Mahmood, T.1
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