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1
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For recent reviews on ynamines and ynamides chemistry, see:
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For recent reviews on ynamines and ynamides chemistry, see:. Hsung R.P., Zificsak C.A., Mulder J.A., Rameshkumar C., and Wei L.-L. Tetrahedron 57 (2001) 7575-7606
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(2001)
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Hsung, R.P.1
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Mulder, J.A.3
Rameshkumar, C.4
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Zhang Y., Hsung R.P., Zhang X., Huang J., Slafer B.W., and Davis A. Org. Lett. 7 (2005) 1047-1050
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Org. Lett.
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Zhang, Y.1
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Davis, A.6
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8
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3142699919
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For selected examples, see:
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For selected examples, see:. Tracey M.R., Zhang Y., Frederick M.O., Mulder J.A., and Hsung R.P. Org. Lett. 6 (2004) 2209-2212
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(2004)
Org. Lett.
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Tracey, M.R.1
Zhang, Y.2
Frederick, M.O.3
Mulder, J.A.4
Hsung, R.P.5
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11
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0000645684
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For selected examples, see:
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For selected examples, see:. Huang J., Xiong H., Hsung R.P., Rameshkumar C., Mulder J.A., and Grebe T.P. Org. Lett. 4 (2002) 2417-2420
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(2002)
Org. Lett.
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Huang, J.1
Xiong, H.2
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Rameshkumar, C.4
Mulder, J.A.5
Grebe, T.P.6
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13
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51049121927
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For recent reviews on gold and platinum catalysis, see:
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For recent reviews on gold and platinum catalysis, see:. Li Z., Brower C., and He C. Chem. Rev. 108 (2008) 3239-3245
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Chem. Rev.
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Arcadi A. Chem. Rev. 108 (2008) 3266-3325
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Arcadi, A.1
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Istrate F., Buzas A., Dias Jurberg I., Odabachian Y., and Gagosz F. Org. Lett. 10 (2008) 925-928
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Hashmi A.S.K., Rudolph M., Bats J.W., Frey W., Rominger F., and Oeser T. Chem. Eur. J. (2008) 6672-6678
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Bats, J.W.3
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Oeser, T.6
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53049098944
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Based on recent investigations by Fürstner and coworkers:
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Based on recent investigations by Fürstner and coworkers:. Fürstner A., and Morency L. Angew. Chem., Int. Ed. (2008) 5030-5033
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Fürstner, A.1
Morency, L.2
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31
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58649104534
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note
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Formula 6a-c in Scheme 3 are mesomeric forms of the same intermediate.
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32
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33646937979
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These reactions conditions are slightly modified compared to those previously reported by Hsung and coworkers, see:
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These reactions conditions are slightly modified compared to those previously reported by Hsung and coworkers, see:. Zhang X., Zhang Y., Huang J., Hsung R.P., Kurtz K.C.M., Oppenheimer J., Petersen M.E., Sagamanove I.K., Shen L., and Tracey M.R. J. Org. Chem. 71 (2006) 4170-4177
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J. Org. Chem.
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Zhang, X.1
Zhang, Y.2
Huang, J.3
Hsung, R.P.4
Kurtz, K.C.M.5
Oppenheimer, J.6
Petersen, M.E.7
Sagamanove, I.K.8
Shen, L.9
Tracey, M.R.10
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33
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2342596963
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Zhang Y., Hsung R.P., Tracey M.R., Kurtz K.C.M., and Vera E.L. Org. Lett. 6 (2004) 1151-1154
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(2004)
Org. Lett.
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Zhang, Y.1
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Tracey, M.R.3
Kurtz, K.C.M.4
Vera, E.L.5
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34
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0037420370
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For other leading references dealing with the Cu(II) catalyzed coupling of bromoalkynes with carbamates, see:
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For other leading references dealing with the Cu(II) catalyzed coupling of bromoalkynes with carbamates, see:. Frederick M.O., Mulder J.A., Tracey M.R., Hsung R.P., Huang J., Kurtz K.C.M., Shen L., and Douglas C.J. J. Am. Chem. Soc. 125 (2003) 2368-2369
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J. Am. Chem. Soc.
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Frederick, M.O.1
Mulder, J.A.2
Tracey, M.R.3
Hsung, R.P.4
Huang, J.5
Kurtz, K.C.M.6
Shen, L.7
Douglas, C.J.8
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37
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Kohnen A.L., Mak X.Y., Lam T.Y., Dunetz J.R., and Danheiser R.L. Tetrahedron (2006) 3815-3822
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Tetrahedron
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Kohnen, A.L.1
Mak, X.Y.2
Lam, T.Y.3
Dunetz, J.R.4
Danheiser, R.L.5
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41
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38349080851
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For gold catalyzed [4+2] cycloadditions of polyenynes, see:
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For gold catalyzed [4+2] cycloadditions of polyenynes, see:. Nieto-Oberhuber C., Péres-Galan P., Herreo-Gomez E., Lautenbach T., Rodriguez C., Lopez S., Bour C., Rosellon A., Cardenas D.J., and Echavarren A.M. J. Am. Chem. Soc. 130 (2008) 269-279
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J. Am. Chem. Soc.
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Nieto-Oberhuber, C.1
Péres-Galan, P.2
Herreo-Gomez, E.3
Lautenbach, T.4
Rodriguez, C.5
Lopez, S.6
Bour, C.7
Rosellon, A.8
Cardenas, D.J.9
Echavarren, A.M.10
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44
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0034703716
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For [4+2] cycloadditions involving furans, see:
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For [4+2] cycloadditions involving furans, see:. Hashmi A.S.K., Frost T.M., and Bats J.W. J. Am. Chem. Soc. 122 (2000) 11553-11554
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J. Am. Chem. Soc.
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Hashmi, A.S.K.1
Frost, T.M.2
Bats, J.W.3
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Hashmi A.S.K., Rudolph M., Weyrauch J.P., Wölfle M., Frey W., and Bats J.W. Angew. Chem., Int. Ed. 44 (2005) 2798-2801
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Hashmi, A.S.K.1
Rudolph, M.2
Weyrauch, J.P.3
Wölfle, M.4
Frey, W.5
Bats, J.W.6
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