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d) A. M. Echavarren, M. Mendez, M. P. Munoz, C. Nevado, B. Martin-Matute, C. Nieto-Oberhuber, D. J. Cardenas, Pure Appl. Chem. 2004, 76, 453-463.
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Echavarren, A.M.1
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Martin-Matute, B.5
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A. S. K. Hashmi, M. Rudolph, J. P. Weyrauch, M. Wölfle, W. Frey, J. W. Bats, Angew. Chem. 2005, 117, 2858-2861;
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A. S. K. Hashmi, T. M. Frost, J. W. Bats, Catal. Today 2001, 72, 19-72.
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22
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33746822109
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Specifically, compound 55 on p. 5761 of ref. [1-1]
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Specifically, compound 55 on p. 5761 of ref. [1-1].
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23
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33746860160
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note
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In the case of the aldehyde, gold is closely related to the reactivity of Tollen's reagent.
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24
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37049141779
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For example, Rh-catalyzed decarbonylation; M. C. Baird, J. T. Mague, J. A. Osborn, G. Wilkinson, J. Chem. Soc (A) 1967, 1347-1360.
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J. Chem. Soc (A)
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Baird, M.C.1
Mague, J.T.2
Osborn, J.A.3
Wilkinson, G.4
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25
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33746809268
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especially p. 71
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For example, see: a) W. H. Perkin, J. Chem. Soc. 1889, 55, 63-90 (especially p. 71);
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Perkin, W.H.1
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26
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33746803979
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especially p. 1014
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b) W. H. Perkin, J. Chem. Soc. 1890, 57, 992-1106 (especially p. 1014).
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J. Chem. Soc.
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Perkin, W.H.1
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27
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33746848785
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Specifically, compounds 80, 83, and 84 in ref. [11]
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Specifically, compounds 80, 83, and 84 in ref. [11].
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30
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0030574774
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c) E. W. Ainscough, A. M. Brodie, R. K. Coll, A. J. A. Mair, J. M. Waters, J. Organomet. Chem. 1996, 509, 259-264;
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Ainscough, E.W.1
Brodie, A.M.2
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Waters, J.M.5
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31
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0000422426
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d) E. W. Ainscough, A.M. Brodie, R. K. Coll, B. A. Coombridge, J. M. Waters, J. Organomet. Chem. 1998, 556, 197-205.
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Ainscough, E.W.1
Brodie, A.M.2
Coll, R.K.3
Coombridge, B.A.4
Waters, J.M.5
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33
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33746832255
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CCDC-283523 (1c), CCDC-283525 (1e), CCDC-283531 (1f), CCDC-283524 (1i), CCDC-283526 (1j), CCDC-283527 (1k), CCDC-281917 (1l), CCDC-283514 (1m), CCDC-283515 (1n), CCDC-283511 (1s), CCDC-281914 (1t), CCDC-283530 (2b), CCDC-283529 (2c), CCDC-283528 (2j), CCDC-283513 (9), CCDC-283512 (11), CCDC-281916 (17), CCDC-281913 (18), CCDC-283519 (19), CCDC-283516 (22), CCDC-283517 (24), CCDC-283518 (26), CCDC-283520 (28), CCDC-283521 (30a), CCDC-283522 (30b), and CCDC-281915 (30 c) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam. ac.uk/data_request/cif.
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35
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33746860955
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Thieme, Stuttgart, specifically p. 42
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For the few examples, see; S. von Angerer, W. Tochtermann, Houben Weyl, Vol. 9d, Thieme, Stuttgart, 1998, pp. 1-64, specifically p. 42.
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Houben Weyl, Vol. 9d
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Von Angerer, S.1
Tochtermann, W.2
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36
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0024821263
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N. L. Allinger, Y. H. Yuh, J.-H. Lii, J. Am. Chem. Soc. 1989, 111, 8551-8566.
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Allinger, N.L.1
Yuh, Y.H.2
Lii, J.-H.3
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0003684555
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Washington University School of Medicine, Saint Louis, MO
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a) J. W. Ponder, TINKER: Software Tools for Molecular Design, 4.2 ed., Washington University School of Medicine, Saint Louis, MO, 2004;
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Ponder, J.W.1
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