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37049066935
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5. Leconte, M.; Jourdan, I.; Pagano, S.; Lefebvre, F.; Basset, J.-M. J. Chem. Soc., Chem. Comm. 1995, 857.
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Leconte, M.1
Jourdan, I.2
Pagano, S.3
Lefebvre, F.4
Basset, J.-M.5
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13
-
-
0013510679
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-
See reference 4
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6. a) See reference 4.
-
-
-
-
14
-
-
0033582714
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b) Hanson, P. R.; Sprott, K. T.; Wrobleski, A. D. Tetrahedron Lett. 1999, 40, 1455.
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Hanson, P.R.1
Sprott, K.T.2
Wrobleski, A.D.3
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15
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84913150907
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7. a) Kafarski, P.; Lejczak, B. Phosphorus, Sulfur, and Silicon 1991, 63, 193.
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Kafarski, P.1
Lejczak, B.2
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19
-
-
0013541226
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-
For the preparation of allylphosphonic acid see reference 4
-
8. a) For the preparation of allylphosphonic acid see reference 4.
-
-
-
-
20
-
-
0013509044
-
-
Vinylphosphonic acid is commercially available from Sigma-Aldrich
-
b) Vinylphosphonic acid is commercially available from Sigma-Aldrich.
-
-
-
-
21
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-
0000200137
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c) For the synthesis of propenyl-phosphonates see: Hirao, T.; Masunaga, T.; Ohshiro, Y.; Agawa, T. Tetrahedron Lett. 1980, 21, 3595.
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Hirao, T.1
Masunaga, T.2
Ohshiro, Y.3
Agawa, T.4
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22
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-
0030818538
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-
9 Conditions described for the reaction of phosphonomonochloridates with amines were used for the preparation of the secondary phosphonamides: Hirschmann, R.; Yager, K. M.; Taylor, C. M.; Witherington, J.; Sprengler, P. A.; Phillips, B. W.; Moore, W.; Smith, A. B. III J. Am. Chem. Soc. 1997, 119, 8177.
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-
Hirschmann, R.1
Yager, K.M.2
Taylor, C.M.3
Witherington, J.4
Sprengler, P.A.5
Phillips, B.W.6
Moore, W.7
Smith A.B. III8
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23
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0000675210
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10. Toluene was used as a solvent to avoid isomerization of the allyl bond in the allylphosphonic acid derivatives: Denmark, S. E.; Kim, J.-H. J. Org. Chem. 1995, 60, 7535.
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-
Denmark, S.E.1
Kim, J.-H.2
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24
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0013510870
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-
note
-
3) δ 25.41.
-
-
-
-
26
-
-
0013536536
-
-
For examples of RCM reactions of N-allyl acrylamides see: references 1d and 12
-
13. For examples of RCM reactions of N-allyl acrylamides see: references 1d and 12.
-
-
-
-
27
-
-
0013553621
-
-
note
-
3) δ 39.74.
-
-
-
-
28
-
-
0013477426
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-
See reference 4
-
15. a) See reference 4.
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-
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