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Various Facets of Organophosphorus
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III Remerciements Je tiens à remer
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3.3.6 Relevance of the Data Assesse
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VII Literature References 115 Compo
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IX Version Abrégée Les composés
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1 Introduction 1 The present thesis
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3 research groups in the field are
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5 However, this mechanism suffers f
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7 At first, a double bromine/lithiu
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10 Although the most frequently emp
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12 The preparation of the latter ph
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protected to its dioxolane derivati
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N (S)-14 1) NBS, THF, - 75 °C 2) -
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3 Alkaline Decomposition of Phospho
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3.2 Alkyl Carbanions Stabilities in
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3.3.1 Mechanistic Discussion on the
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25 The assumption reported by these
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27 However, in the eventuality of a
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29 To prepare tertiary phosphines b
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31 Table 4. Mixed tertiary alkylpho
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33 were comparable to those obtaine
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35 led to the formation of di-tert-
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37 depending on the alkyl substitue
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39 4 A Novel Access to Atropisomeri
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41 Since the homocoupling of the ha
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43 Few other attempts to selectivel
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45 The second phenol ether 36 was f
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47 The enantiomeric purity was chec
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49 A second purpose of this derivat
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51 substrates considered. In conseq
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53 Single-crystal X-ray analysis of
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55 To convert atropisomer Ia into I
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57 This finally allows one to use t
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the steric bulk and charge delocali
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61 To check the reproducibility of
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63 Figure 9. Full lineshape analysi
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66 suitably substituted dilithiobip
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Experimental Part
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70 deuterochloroform (CDCl3) unless
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- Page 96 and 97: 1 H NMR: δ = 6.96 (s, 3 H), 6.94 (
- Page 98 and 99: 76 C21H21O9P (448.36) calcd. C 56.2
- Page 100 and 101: 78 C12H12BrN (250.13) calcd. C 57.6
- Page 102 and 103: 80 C13H13NO2 (215.25) calcd. C 72.5
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- Page 116 and 117: 94 13 C NMR: δ = 40.8 (d, J = 3 Hz
- Page 118 and 119: 96 31 P NMR settings: It is known t
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- Page 140 and 141: 116 Conference Proceedings, Naples,
- Page 142 and 143: 118 [ 70] J. Drowart, C.E. Myers, R
- Page 146 and 147: 122 [170] B.H. Lipshutz, F. Kayser,
- Page 148: 124 [212] M. Schlosser, in Organome
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