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(a) Yamaguchi, K.; Mori, K.; Mizugaki, T.; Ebitani, K.; Kaneda, K. J. Am. Chem. Soc. 2000, 122, 7144.
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10
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0141492987
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note
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6 and NaOTf were used instead of silver salts to avoid an interference of insoluble AgCl.
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11
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0141604605
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note
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See Supporting Information.
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12
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0000484465
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For some recent reports on Lewis acid-catalyzed Diels-Alder reaction, see: (a) Odenkirk, W.; Rheingold, A.-L.; Bosnich, B. J. Am. Chem. Soc. 1992, 114, 6392.
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Odenkirk, W.1
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0141492986
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(c) Pigant, K.; Vallotto, J.; Pinna, F.; Strukul, G. Organometallics 2000, 19, 5160.
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Organometallics
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Strukul, G.4
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15
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(d) Kündig, E. P.; Saudan, C. M.; Alenzra, V.; Viton, F.; Bernardinelli, G. Angew. Chem., Int. Ed. 2001, 40, 4481.
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Kündig, E.P.1
Saudan, C.M.2
Alenzra, V.3
Viton, F.4
Bernardinelli, G.5
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17
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0000587457
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For leading references of transition metal complex-catalyzed aldol reaction of nitriles, see: (a) Lin, Y.; Zhu, X.; Xiang, M. J. Organomet. Chem. 1993, 448, 215.
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(b) Hirano, M.; Ito, Y.; Hirai, M.; Fukuoka, A.; Komiya, S. Chem. Lett. 1993, 2057.
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(c) Nemoto, H.; Kubota, Y.; Yamamoto, Y. J. Chem. Soc., Chem. Commun. 1994, 1665.
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(d) Murahashi, S.-I.; Naota, T.; Taki, H.; Mizuno, M.; Takaya, H.; Komiya, S.; Mizuho, Y.; Oyasato, N.; Hiraoka, M.; Hirano, M.; Fukuoka, A. J. Am. Chem. Soc. 1995, 117, 12436.
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Fukuoka, A.11
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21
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0001058494
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It is said that the base abstracts a proton of isonitriles coordinating to the metals, see: (a) Nesper, R.; Pregosin, P. S.; Püntener, K.; Wörle, M. Helv. Chim. Acta 1993, 76, 2239.
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Nesper, R.1
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Püntener, K.3
Wörle, M.4
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26
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0141827675
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note
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Steric repulsion between the phenyl groups of 4a and the isocyano moiety bound to the Ru phosphate complex in synclinal configuration severely limits the formation of cis-isomer.
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