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For selected recent reviews on gold catalysis, see:
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For recent reviews and reports of transition metal catalyzed hydrofunctionalization, see:
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Hashmi, A.S.K.1
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26
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34247877815
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For a recent critical review on gold catalysis, which pointed out that proton is a real catalyst in some reactions, see:
-
For a recent critical review on gold catalysis, which pointed out that proton is a real catalyst in some reactions, see:. Hashmi A.S.K. Catal. Today 122 (2007) 211
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Hashmi, A.S.K.1
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58949083775
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For recent reviews of transition metal catalyzed hydroamination, see:
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For recent reviews of transition metal catalyzed hydroamination, see:
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38
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33847198325
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Buil M.L., Esteruelas M.A., Lopez A.M., Mateo A.C., and Onate E. Organometallics 26 (2007) 554
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40
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58949083774
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See, Ref. 2a. For other thermochemical reviews, see:
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See, Ref. 2a. For other thermochemical reviews, see:
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58949086725
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For recent reviews of early transition metal catalyzed hydroamination, see:
-
For recent reviews of early transition metal catalyzed hydroamination, see:
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54
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58949083773
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For very recent examples, see:
-
For very recent examples, see:
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56
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48149105517
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Lavallo V., Frey G.D., Donnadieu B., Soleilhavoup M., and Bertrand G. Angew. Chem., Int. Ed. 47 (2008) 5224
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9644309177
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Recently, we found that the use of olefin enhanced the reaction rate in the platinum-catalyzed intramolecular carboalkoxylation of alkynes; see:
-
Recently, we found that the use of olefin enhanced the reaction rate in the platinum-catalyzed intramolecular carboalkoxylation of alkynes; see:. Nakamura I., Bajracharya G.B., Wu H., Oishi K., Mizushima Y., Gridnev I.D., and Yamamoto Y. J. Am. Chem. Soc. 126 (2004) 15423
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58949094617
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For other examples of gold-mediated racemization of allenes, see:
-
For other examples of gold-mediated racemization of allenes, see:
-
-
-
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65
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58949092705
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For examples of intramolecular gold-catalyzed hydroamination with aliphatic amine bearing substrates, see:
-
For examples of intramolecular gold-catalyzed hydroamination with aliphatic amine bearing substrates, see:
-
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68
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58949097635
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See also Refs. 5g and 7a.
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See also Refs. 5g and 7a.
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58949095866
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For selected recent examples, see:
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For selected recent examples, see:
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Kirsch S.F., Binder J.T., Crone B., Duschek A., Haug T.T., Litbert C., and Menz H. Angew. Chem., Int. Ed. 46 (2007) 2310
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103
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25844453872
-
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+ -OTf according to Echavarren's method and used it for the hydroamination of 1a. Product 3a was obtained in 71% yield, indicating that the cationic gold complex was a catalytic species. See: See also 14a-c
-
+ -OTf according to Echavarren's method and used it for the hydroamination of 1a. Product 3a was obtained in 71% yield, indicating that the cationic gold complex was a catalytic species. See:. Nieto-Oberhuber C., López S., Muñoz M.P., Cárdenas D.J., Buñuel E., Nevado C., and Echavarren A.M. Angew. Chem., Int. Ed. 44 (2005) 6146 See also 14a-c
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Nieto-Oberhuber, C.1
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Alcock, N.W.1
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107
-
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58949096740
-
-
note
-
The progress of this reaction could not be monitored by TLC or GC-MS, because of low boiling point of the starting allene. Thus, the reaction was stopped after 24 h without following the reaction progress.
-
-
-
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109
-
-
58949086724
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For a recent review of hydroalkoxylation, see Ref. 5j. For recent reviews of hydration, see:
-
For a recent review of hydroalkoxylation, see Ref. 5j. For recent reviews of hydration, see:
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110
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34247592139
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Brückner R. (Ed), Thieme, Stuttgart
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Schulz, M.; Teles, J. H. WO Patent 9721648, 1997;
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Schulz, M.; Teles, J. H. WO Patent 9721648, 1997;
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-
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118
-
-
58949092704
-
-
note
-
The reaction was very exothermic, and resulted in the formation of a complex mixture of products. The corresponding allylic ether was not detected by GC-MS and NMR. To make the reaction conditions milder, the hydroalkoxylation was carried out under diluted condition in toluene, but the corresponding product was not detected. However, Widenhoefer and Zhang succeeded in the hydroalkoxylation of phenol (Ref. 27a).
-
-
-
-
119
-
-
58949093692
-
-
note
-
The progress of this reaction could not be monitored by TLC or GC-MS, because of low boiling points of the starting allene and product. Thus, the reaction was stopped after 24 h. Isolation of the product was also very difficult for the same reason as above, and therefore the NMR yield was calculated using dibromomethane as an internal standard.
-
-
-
-
120
-
-
27844460180
-
-
For the study of gold-mediated hydroalkoxylation of alkynes in gas-phase reaction and its theoretical study, see:
-
For the study of gold-mediated hydroalkoxylation of alkynes in gas-phase reaction and its theoretical study, see:. Roithová J., Hrušák J., Schröder D., and Schwarz H. Inorg. Chim. Acta 358 (2005) 4287
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121
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58949089652
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1-allyl gold (not π-allyl gold) was known, see:
-
1-allyl gold (not π-allyl gold) was known, see:
-
-
-
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123
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0006897944
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Sone T., Ozaki S., Kasuga N.C., Fukuoka A., and Komiya S. Bull. Chem. Soc. Jpn. 68 (1995) 1523
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125
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58949089653
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The methods for the synthesis of gold-phosphine complexes, see:
-
The methods for the synthesis of gold-phosphine complexes, see:
-
-
-
-
128
-
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58949098512
-
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The method for the synthesis of phosphines, see:
-
The method for the synthesis of phosphines, see:
-
-
-
-
130
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0036165903
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Brauer D.J., Hingst M., Kottsieper K.W., Liek C., Nickel T., Tepper M., Stelzer O., and Sheldrick W.S. J. Organomet. Chem. 645 (2002) 14
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Reinius, H.; Krause, O.; Riihimäki, H.; Laitinen, R.; Pursiainen, J. WO/20448, 2002.
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Reinius, H.; Krause, O.; Riihimäki, H.; Laitinen, R.; Pursiainen, J. WO/20448, 2002.
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