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5
-
-
57649084012
-
-
Further examples of carbene reactions with N-H bonds have already been published:
-
Further examples of carbene reactions with N-H bonds have already been published:
-
-
-
-
7
-
-
57649093705
-
-
With electrophilic metal carbenes, see:
-
With electrophilic metal carbenes, see:
-
-
-
-
11
-
-
57649110717
-
-
With nucleophilic carbenes:
-
With nucleophilic carbenes:
-
-
-
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12
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34247543841
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Frey G.D., Lavallo V., Donnadieu B., Schoeller W.W., and Bertrand G. Science 316 (2007) 439
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13
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55049110189
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Mieusset J.-L., Billing P., Bespokoev A., Pacar M., Abraham M., Arion V.B., and Brinker U.H. Eur. J. Org. Chem. (2008) 5336
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Bespokoev, A.3
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Abraham, M.5
Arion, V.B.6
Brinker, U.H.7
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15
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84926985489
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Marchand A.P., and Lehr R.E. (Eds), Academic, New York, NY p 118
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Jones W.M., and Brinker U.H. In: Marchand A.P., and Lehr R.E. (Eds). Pericyclic Reactions Vol. 1 (1977), Academic, New York, NY p 118
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2542495781
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Moss R.A., Platz M.S., and Jones Jr. M. (Eds), Wiley, Hoboken pp 298-306
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Reactive Intermediate Chemistry
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Jones Jr., M.1
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Matthews W.S., Bares J.E., Bartmess J.E., Bordwell F.G., Cornforth F.J., Drucker G.E., Margolin Z., McCallum R.J., McCollum G.J., and Vanier N.R. J. Am. Chem. Soc. 97 (1975) 7006
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41
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0033403533
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Arduengo III A.J., Calabrese J.C., Davidson F., Rasika Dias H.V., Goerlich J.R., Krafczyk R., Marshall W.J., Tamm M., and Schmutzler R. Helv. Chim. Acta 82 (1999) 2348
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Korotkikh N.I., Rayenko G.F., Shvaika O.P., Pekhtereva T.M., Cowley A.H., Jones J.N., and Macdonald C.L.B. J. Org. Chem. 68 (2003) 5762
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Macdonald, C.L.B.7
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43
-
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57649099500
-
-
For further examples, see:
-
For further examples, see:
-
-
-
-
44
-
-
37049108809
-
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Okamoto K., Kitagawa T., Takeuchi K., Komatsu K., and Takahashi K. J. Chem. Soc., Chem. Commun. (1985) 173
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0035938263
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Kitagawa T., Tanaka T., Murakita H., Nishikawa A., and Takeuchi K. Tetrahedron 57 (2001) 3537
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Kitagawa, T.1
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Takeuchi, K.5
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50
-
-
57649100428
-
-
note
-
2,7]undec-9-ene systems. According to the IUPAC Gold Book, the description anti should be used when the group is oriented away from the lowest numbered bridge.
-
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Scalmani, G.17
Rega, N.18
Petersson, G.A.19
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Ehara, M.22
Toyota, K.23
Fukuda, R.24
Hasegawa, J.25
Ishida, M.26
Nakajima, T.27
Honda, Y.28
Kitao, O.29
Nakai, H.30
Klene, M.31
Li, X.32
Knox, J.E.33
Hratchian, H.P.34
Cross, J.B.35
Adamo, C.36
Jaramillo, J.37
Gomperts, R.38
Stratmann, R.E.39
Yazyev, O.40
Austin, A.J.41
Cammi, R.42
Pomelli, C.43
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Ayala, P.Y.45
Morokuma, K.46
Voth, G.A.47
Salvador, P.48
Dannenberg, J.J.49
Zakrzewski, V.G.50
Dapprich, S.51
Daniels, A.D.52
Strain, M.C.53
Farkas, O.54
Malick, D.K.55
Rabuck, A.D.56
Raghavachari, K.57
Foresman, J.B.58
Ortiz, J.V.59
Cui, Q.60
Baboul, A.G.61
Clifford, S.62
Cioslowski, J.63
Stefanov, B.B.64
Liu, G.65
Liashenko, A.66
Piskorz, P.67
Komaromi, I.68
Martin, R.L.69
Fox, D.J.70
Keith, T.71
Al-Laham, M.A.72
Peng, C.Y.73
Nanayakkara, A.74
Challacombe, M.75
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Johnson, B.77
Chen, W.78
Wong, M.W.79
Gonzalez, C.80
Pople, J.A.81
more..
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60
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57649093702
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note
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CCDC 704291 (for 10) contains 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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