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1
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0003464704
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Murai, M, Ed, Springer: Berlin
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(a) Murai, M.; Ito, Y. Activation of Un reactive Bonds and Organic Synthesis; Murai, M., Ed.; Springer: Berlin, 1999; pp 99-129.
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(1999)
Activation of Un reactive Bonds and Organic Synthesis
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Murai, M.1
Ito, Y.2
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5
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0037184466
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(c) Murakami, M.; Itahashi, T.; Ito, Y. J. Am. Chem. Soc. 2002, 124, 13976-13977.
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J. Am. Chem. Soc
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Murakami, M.1
Itahashi, T.2
Ito, Y.3
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(a) Nakao, Y.; Oda, S.; Hiyama, T. J. Am. Chem. Soc. 2004, 126, 13904-13905.
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J. Am. Chem. Soc
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Nakao, Y.1
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8
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0037013636
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(a) Jun, C. -H.; Moon, C. W.; Lee, D.-Y. Chem. Eur. J. 2002, 8, 2422-2428.
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Chem. Eur. J
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Jun, C.-H.1
Moon, C.W.2
Lee, D.-Y.3
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3242702956
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(b) Wakui, H.; Kawasaki, S.; Satoh, T.; Miura, M.; Nomura, M. J. Am. Chem. Soc. 2004, 126, 8658-8659.
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Wakui, H.1
Kawasaki, S.2
Satoh, T.3
Miura, M.4
Nomura, M.5
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10
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58149192392
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Few examples on the cleavage of an unreactive carbon-carbon bond are known, see
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Few examples on the cleavage of an unreactive carbon-carbon bond are known, see:
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11
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33748356066
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(a) Kuninobu, Y.; Kawata, A.; Takai, K. J. Am. Chem. Soc. 2006, 128, 11368-11369.
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(2006)
J. Am. Chem. Soc
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Kuninobu, Y.1
Kawata, A.2
Takai, K.3
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14
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58149191810
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Though Cu(OAc)2 and Cu(OTf)2 were as effective as CuI, we chose CuI as a catalyst for this reaction due to its stability and low price. Cu bronze, CuCl, CuO, and CU2O were less effective. © 2008 American Chemical Society
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2O were less effective. © 2008 American Chemical Society.
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15
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8644263988
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It is known that the α-position of ketone was easily nitrosated by nitrites, see: Rüedi, G.; Oberli, M, A.; Nagel, M.; Weymuth, C.; Hansen, H.-J. Synlett 2004, 13, 2315-2318.
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It is known that the α-position of ketone was easily nitrosated by nitrites, see: Rüedi, G.; Oberli, M, A.; Nagel, M.; Weymuth, C.; Hansen, H.-J. Synlett 2004, 13, 2315-2318.
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16
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58149184253
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For reviews, see
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For reviews, see:
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17
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4644319315
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(a) ten Brink, G. J.; Arends, I. W. C. E.; Sheldon, R. A. Chem. Rev. 2004,104, 4105-4124.
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(2004)
Chem. Rev
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ten Brink, G.J.1
Arends, I.W.C.E.2
Sheldon, R.A.3
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19
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84986409474
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Shin, H. H.; Park, Y. J.; Kim, Y. H. Heteroatom Chem. 1993, 4, 259-262.
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(1993)
Heteroatom Chem
, vol.4
, pp. 259-262
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Shin, H.H.1
Park, Y.J.2
Kim, Y.H.3
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20
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58149196742
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It is known that nitrite is reduced by copper complex such as copper-containig nitrite reductase to afford a Cu-NO complex, see
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It is known that nitrite is reduced by copper complex such as copper-containig nitrite reductase to afford a Cu-NO complex, see:
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21
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2442604589
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(a) Tocheva, E. I.; Rosell, F. I.; Mauk, A. G.; Murphy, M. E. P. Science 2004, 304, 867-870.
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(2004)
Science
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, pp. 867-870
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Tocheva, E.I.1
Rosell, F.I.2
Mauk, A.G.3
Murphy, M.E.P.4
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22
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4844226192
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(b) Burg, A.; Lozinsky, E.; Cohen, H.; Meyerstein. D. Eur. J. Inorg. Chem. 2004, 367, 5-3680.
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(2004)
Eur. J. Inorg. Chem
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Burg, A.1
Lozinsky, E.2
Cohen, H.3
Meyerstein, D.4
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23
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58149196743
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An example of the insertion of an alkoxy copper complex to the carbonyl group exists, see: Kubota, M, Yamamoto, T, Yamamoto, A. Bull. Chem. Soc. Jpn. 1979, 52, 146-150
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An example of the insertion of an alkoxy copper complex to the carbonyl group exists, see: Kubota, M.; Yamamoto, T.; Yamamoto, A. Bull. Chem. Soc. Jpn. 1979, 52, 146-150.
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24
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58149198137
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This process would be the rate-determining step of this reaction
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This process would be the rate-determining step of this reaction.
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