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Hall, A.1
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Giblin, G.M.P.3
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2
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67649318372
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WO 2006066968, 2006; 83231
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(b) Giblin, G. M. P.; Hall, A.; Hurst, D. N.; Rawlings, D. A.; Scoccitti, T. WO 2006066968, 2006; Chem. Abstr. 2006, 145, 83231.
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Chem. Abstr.
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Giblin, G.M.P.1
Hall, A.2
Hurst, D.N.3
Rawlings, D.A.4
Scoccitti, T.5
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4
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0000254267
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(b) Casiraghi, G.; Cornia, M.; Rassu, G. J. Org. Chem. 1988, 53, 4919.
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Casiraghi, G.1
Cornia, M.2
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5
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(c) Bigi, F.; Casnati, G.; Sartori, G.; Araldi, G.; Bocelli, G. Tetrahedron Lett. 1989, 30, 1121.
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(1989)
Tetrahedron Lett.
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Bigi, F.1
Casnati, G.2
Sartori, G.3
Araldi, G.4
Bocelli, G.5
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7
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0000603443
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(e) Saimoto, H.; Yoshida, K.; Tetsuya, M.; Morimoto, M.; Sashiwa, H.; Shigemasa, Y. J. Org. Chem. 1996, 61, 6768.
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Saimoto, H.1
Yoshida, K.2
Tetsuya, M.3
Morimoto, M.4
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Shigemasa, Y.6
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9
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33846599336
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(g) Rondot, C.; Retailleau, P.; Zhu, J. Org. Lett. 2007, 9, 247.
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Rondot, C.1
Retailleau, P.2
Zhu, J.3
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11
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0020851963
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For a review, see
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For a review, see: Casnati, G.; Casiraghi, G.; Pochini, A.; Sartori, G.; Ungaro, R. Pure Appl. Chem. 1983, 55, 1677.
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Pure Appl. Chem.
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Casnati, G.1
Casiraghi, G.2
Pochini, A.3
Sartori, G.4
Ungaro, R.5
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12
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0030750821
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For leading references, see
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For leading references, see: Bocelli, G.; Cantoni, A.; Sartori, G.; Maggi, R.; Bigi, F. Chem. Eur. J. 1997, 3, 1269.
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Chem. Eur. J.
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Bocelli, G.1
Cantoni, A.2
Sartori, G.3
Maggi, R.4
Bigi, F.5
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13
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37049138314
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For selected examples, see
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For selected examples, see: (a) Casiraghi, G.; Casnati, G.; Cornia, M.; Sartori, G.; Ungaro, R. J. Chem. Soc. Perkin Trans. 1 1974, 2077.
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(1974)
J. Chem. Soc. Perkin Trans. 1
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Casiraghi, G.1
Casnati, G.2
Cornia, M.3
Sartori, G.4
Ungaro, R.5
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14
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0010689356
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(b) Casnati, G.; Colli, M.; Pochini, A.; Ungaro, R. Chim. Ind. (Milan) 1977, 59, 764.
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Chim. Ind. (Milan)
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Casnati, G.1
Colli, M.2
Pochini, A.3
Ungaro, R.4
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15
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37049098125
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(c) Casiraghi, G.; Casnati, G.; Cornia, M.; Pochini, M.; Puglia, G.; Sartori, G.; Ungaro, R. J. Chem. Soc., Perkin Trans. 1 1978, 318.
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J. Chem. Soc., Perkin Trans. 1
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Casiraghi, G.1
Casnati, G.2
Cornia, M.3
Pochini, M.4
Puglia, G.5
Sartori, G.6
Ungaro, R.7
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16
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33845560756
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(d) Sartori, G.; Casiraghi, G.; Bolzoni, L.; Casnati, G. J. Org. Chem. 1979, 44, 803.
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Sartori, G.1
Casiraghi, G.2
Bolzoni, L.3
Casnati, G.4
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17
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0007317744
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(e) Casiraghi, G.; Casnati, G.; Dradi, E.; Messori, R.; Sartori, G. Tetrahedron 1979, 35, 2061.
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(1979)
Tetrahedron
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Casiraghi, G.1
Casnati, G.2
Dradi, E.3
Messori, R.4
Sartori, G.5
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18
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37049103965
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(f) Casiraghi, G.; Casnati, G.; Pochini, A.; Ungaro, R. J. Chem. Soc., Perkin Trans. 1 1982, 805.
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(1982)
J. Chem. Soc., Perkin Trans. 1
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Casiraghi, G.1
Casnati, G.2
Pochini, A.3
Ungaro, R.4
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20
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0027933843
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Sartori, G.; Maggi, R.; Bigi, F.; Arienti, A.; Porta, C.; Predieri, G. Tetrahedron 1994, 50, 10587.
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(1994)
Tetrahedron
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Sartori, G.1
Maggi, R.2
Bigi, F.3
Arienti, A.4
Porta, C.5
Predieri, G.6
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21
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67649328533
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note
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2O on scale is complicated by its high volatility and flammability, MTBE is a much preferred alternative.
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22
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0000059198
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2 to promote selective orthoformylation of phenols, see
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2 to promote selective orthoformylation of phenols, see: (a) Hofslokken, N. U.; Skattebol, L. Acta Chem. Scand. 1999, 53, 258.
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(1999)
Acta Chem. Scand.
, vol.53
, pp. 258
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Hofslokken, N.U.1
Skattebol, L.2
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24
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30144431765
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This becomes the main reaction pathway if phenol is omitted from the reaction mixture. For a recent report of a similar process, see
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This becomes the main reaction pathway if phenol is omitted from the reaction mixture. For a recent report of a similar process, see: Abaee, M. S.; Sharifi, R.; Mojtahedi, M. M. Org. Lett. 2005, 7, 5893.
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(2005)
Org. Lett.
, vol.7
, pp. 5893
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Abaee, M.S.1
Sharifi, R.2
Mojtahedi, M.M.3
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25
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67649326054
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note
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2, EtOH, EtOAc, i-PrOAc, 2-methyltetrahydrofuran, THF, α,α,α-trifluorotoluene, and sulfolane.
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26
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0041737791
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2 does not have a significant effect on the rate of the desired reduction but greatly reduces the rate of competitive dechlorination. For a report on the use of zinc halides to modulate the activity of hydrogenation catalysts, see
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2 does not have a significant effect on the rate of the desired reduction but greatly reduces the rate of competitive dechlorination. For a report on the use of zinc halides to modulate the activity of hydrogenation catalysts, see: Wu, G.; Huang, M.; Richards, M.; Poirier, M.; Wen, X.; Draper, R. W. Synthesis 2003, 1657.
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(2003)
Synthesis
, pp. 1657
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Wu, G.1
Huang, M.2
Richards, M.3
Poirier, M.4
Wen, X.5
Draper, R.W.6
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