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1
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0000038757
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See for example: (a) Y. Miquel, A. Igau, B. Donnadieu, J.-P. Majoral, N. Pirio, P. Meunier, J. Am. Chem. Soc. 120 (1998) 3504.
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(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 3504
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-
Miquel, Y.1
Igau, A.2
Donnadieu, B.3
Majoral, J.-P.4
Pirio, N.5
Meunier, P.6
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2
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0040008982
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(b) Cénac N., Chrostowska A., Sotiropoulos J.-M., Donnadieu B., Igau A., Pfister-Guillouzo G., Majoral J.-P., Organometallics 17 (1997) 4551.
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(1997)
, vol.17
, pp. 4551
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Cénac, N.1
Chrostowska, A.2
Sotiropoulos, J.-M.3
Donnadieu, B.4
Igau, A.5
Pfister-Guillouzo, G.6
Majoral, J.-P.7
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3
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0002563399
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(c) Zablocka M., Igau A., Donnadieu B., Majoral J.-P., Skowronska A., Meunier P., Chem. Commun. (1997) 1239.
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(1997)
Chem. Commun.
, pp. 1239
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Zablocka, M.1
Igau, A.2
Donnadieu, B.3
Majoral, J.-P.4
Skowronska, A.5
Meunier, P.6
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4
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0000183222
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(d) Mahieu A., Miquel Y., Igau A., Donnadieu B., Majoral J.-P., Organometallics 16 (1997) 3086.
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(1997)
Organometallics
, vol.16
, pp. 3086
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Mahieu, A.1
Miquel, Y.2
Igau, A.3
Donnadieu, B.4
Majoral, J.-P.5
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5
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0030905759
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and references therein
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(e) Dupuis L., Pirio N., Meunier P., Igau A., Donnadieu B., Majoral J.-P., Angew. Chem. Int. Ed. Engl. 36 (1997) 987 and references therein.
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(1997)
Angew. Chem. Int. Ed. Engl.
, vol.36
, pp. 987
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Dupuis, L.1
Pirio, N.2
Meunier, P.3
Igau, A.4
Donnadieu, B.5
Majoral, J.-P.6
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6
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0342866532
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(a) Cénac N., Zablocka M., Igau A., Majoral J. P., Skowronska A., J. Org. Chem. 61 (1996) 796.
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(1996)
J. Org. Chem.
, vol.61
, pp. 796
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Cénac, N.1
Zablocka, M.2
Igau, A.3
Majoral J., P.4
Skowronska, A.5
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7
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3042750574
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(b) N. Cénac, M. Zablocka, A. Igau, G. Commenges, J. P. Majoral, A. Skowronska, Organometallics 15 (1996) 1208.
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(1996)
Organometallics
, vol.15
, pp. 1208
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Cénac, N.1
Zablocka, M.2
Igau, A.3
Commenges, G.4
Majoral J., P.5
Skowronska, A.6
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11
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33947294608
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The turnstile mechanism is sometimes alternatively invoked, but for the triquinphosphoranes the pseudo-rotation according Berry is by far the most appropriated in the sense of symmetrical factors and due to the structural dependence of five membered rings:
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(b) K. Mislow, Acc. Chem. Res. 3 (1970) 321. The turnstile mechanism is sometimes alternatively invoked, but for the triquinphosphoranes the pseudo-rotation according Berry is by far the most appropriated in the sense of symmetrical factors and due to the structural dependence of five membered rings:
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(1970)
Acc. Chem. Res.
, vol.3
, pp. 321
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Mislow, K.1
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12
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0001052145
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The topological equivalence between Berry and turnstile pseudo-rotation has been addressed
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(c) I. Ugi, D. Marquarding, H. Klusacek, P. Gillespie, F. Ramirez, Acc. Chem. Res. 4 (1971) 288. The topological equivalence between Berry and turnstile pseudo-rotation has been addressed:
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(1971)
Acc. Chem. Res.
, vol.4
, pp. 288
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Ugi, I.1
Marquarding, D.2
Klusacek, H.3
Gillespie, P.4
Ramirez, F.5
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14
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0001243019
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For the nomenclature of chiral pentacoordinated compounds see: The sense of chirality can be specified by viewing the idealized TBP structure along its apical axis in the orientation which places nearer the viewer the apical substituent which has the higher priority rank in the CIP nomenclature scheme. The priority ranking of the equatorial ligands using the CIP conventions results in order decreasing priority which can be recognized by the viewer as being clockwise (R) or counterclokwise (S)
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For the nomenclature of chiral pentacoordinated compounds see: (a) J.C. Martin, T.M. Balthazor, J. Am. Chem. Soc. 99 (1977) 152. The sense of chirality can be specified by viewing the idealized TBP structure along its apical axis in the orientation which places nearer the viewer the apical substituent which has the higher priority rank in the CIP nomenclature scheme. The priority ranking of the equatorial ligands using the CIP conventions results in order decreasing priority which can be recognized by the viewer as being clockwise (R) or counterclokwise (S).
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(1977)
J. Am. Chem. Soc.
, vol.99
, pp. 152
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Martin, J.C.1
Balthazor, T.M.2
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18
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85037799324
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have recently obtained an X-ray diffraction structure of the triquinphosphorane deriving from N,N′-bis[(-)-norephedrine]ethylene. In this structure, the phosphorus atom adopts a TBP geometry with a nitrogen atom in apical position and the five membered rings in the apical-equatorial positions
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(d) Contreras et al. have recently obtained an X-ray diffraction structure of the triquinphosphorane deriving from N,N′-bis[(-)-norephedrine]ethylene. In this structure, the phosphorus atom adopts a TBP geometry with a nitrogen atom in apical position and the five membered rings in the apical-equatorial positions.
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Contreras1
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20
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85037790224
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C. Doctoral Thesis no. 96AIX30083, University Aix-Marseille 3, France
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C. Marchi, C. Doctoral Thesis no. 96AIX30083, University Aix-Marseille 3, France, 1996.
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(1996)
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Marchi, C.1
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23
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84985494070
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The place of transition metals in organic synthesis
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D.W. Slocum (Ed.)
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(b) M.D. Rausch, W. H. Boon, H. G. Alt, The place of transition metals in organic synthesis, in: D.W. Slocum (Ed.), Annals of the New York Academy of Sciences, vol. 295, 1977, p. 103.
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(1977)
Annals of the New York Academy of Sciences
, vol.295
, pp. 103
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M.D. Rausch1
W. H. Boon2
H. G. Alt3
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