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(c) R. P. Arshinova, A. Ch. Plyamovatyi, R. A. Kadyrov, S. G. Gnevashev and B. A. Arbusov, Phosphorus Sulfur Silicon Relat. Elem., 41, 449 (1989);
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0043203457
-
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note
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The numbering system adopted corresponds to the Chem. Abstr. numbering of the analogous 12H-dibenzo[d.g][1,3,2]dioxaphosphocin ring system. The C(12) bridging carbon atom corresponds to C(10) in the X-Ray crystal structure of 3.
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31
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Pergamon: Oxford
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The two-bond geminal coupling constant is presumed to be negative, see L. M. Jackman and S. Sternhell, "Applications of Nuclear Magnetic Resonance Spectroscopy in Organic Chemistry," 2nd ed., Pergamon: Oxford, 1969, pp. 270-279.
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R. R. Fraser, M. A. Raza, R. N. Renaud and R. B. Layton, Can J. Chem., 53, 167 (1975).
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W. Lwowski, ed., Pergamon: Oxford
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J. A. Moore and F. A. Anet, in "Comprehensive Heterocyclic Chemistry Vol. 7," W. Lwowski, ed., Pergamon: Oxford, 1984, pp. 653-707.
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Comprehensive Heterocyclic Chemistry Vol. 7
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Anet, F.A.2
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B. A. Arbuzov, V. V. Klochkov, L. V. Egorova, K. A. Il'yasov and R. P. Arshinova, Dokl. Akad. Nauk SSSR (Engl. Transl.), 305, 80 (1989).
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41
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ACS Monograph 177: Washington, D.C.
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For a review on calculations on medium-sized carbocyclics, see U. Burkert and N. L. Allinger, Molecular Mechanics; ACS Monograph 177: Washington, D.C., 1982.
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43
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R. O. Day, J. M. Holmes, A. C. Sau and R. R. Holmes, Inorg. Chem., 21, 281 (1982).
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S. E. Denmark, R. T. Jacobs, G. Dai-Ho and S. Wilson, Organometallics, 9, 3015 (1990).
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Denmark, S.E.1
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45
-
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0043203462
-
-
note
-
The magnitude of the geminal coupling constant for the C(12) methylene protons (14 Hz) in 4 is consistent with the solution conformation being either a TB or a BC in rapid equilibration with a TB conformer.
-
-
-
-
46
-
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0003969438
-
-
The Chemical Society: Special Publication No. 11, and Supplement; Special Publication No. 18
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(a) Tables of Interatomic Distances and Configuration in Molecules and Ions, The Chemical Society: Special Publication No. 11, 1958 and Supplement; Special Publication No. 18, 1965.
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Tables of Interatomic Distances and Configuration in Molecules and Ions
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-
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47
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10044282108
-
-
Quite recently, Holmes has reported that an electronic effect (coordination of sulfur to silicon) in addition to a steric effect may be responsible for the BB conformation found for analogs of 5, see T. K. Prakasha, S. Srinivasan, A. Chandrasekaran, R. O. Day and R. R. Holmes, J. Am. Chem. Soc., 117, 10003 (1995).
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Prakasha, T.K.1
Srinivasan, S.2
Chandrasekaran, A.3
Day, R.O.4
Holmes, R.R.5
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