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6
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0004111873
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Ager D.J. (Ed), Wiley, New York, NY
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In: Ager D.J. (Ed). Umpoled Synthons (1987), Wiley, New York, NY
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8
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4243712434
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Chem. Abstr. 45 (1951) 5148
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(1951)
Chem. Abstr.
, vol.45
, pp. 5148
-
-
-
11
-
-
38349055001
-
-
Carbenes in acyloin type couplings:
-
-
-
-
22
-
-
84890988742
-
-
Dalko P.I. (Ed), Wiley-VCH, Weinheim
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Enders D., Balensiefer T., and Niemeier O. In: Dalko P.I. (Ed). Enantioselective Organocatalysis (2007), Wiley-VCH, Weinheim 331
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Enantioselective Organocatalysis
, pp. 331
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-
Enders, D.1
Balensiefer, T.2
Niemeier, O.3
-
23
-
-
38348999341
-
-
Carbenes in Stetter couplings:
-
-
-
-
31
-
-
38349071016
-
-
Dalko P.I. (Ed), Wiley-VCH, Weinheim
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Enders D., Balensiefer T., and Niemeier O. In: Dalko P.I. (Ed). Enantioselective Organocatalysis (2007), Wiley-VCH, Weinheim 338
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, pp. 338
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Enders, D.1
Balensiefer, T.2
Niemeier, O.3
-
32
-
-
38349036335
-
-
Metallophosphites in acyloin type couplings:
-
-
-
-
34
-
-
38349058601
-
-
Nahm M.R., Linghu X., Potnick J.R., Yates C.M., White P.S., and Johnson J.S. Angew. Chem. 117 (2005) 2429
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Nahm, M.R.1
Linghu, X.2
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Yates, C.M.4
White, P.S.5
Johnson, J.S.6
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43
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Rassolov, V.A.1
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Redfern, P.C.4
Curtiss, L.A.5
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44
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0004238823
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Experimentally, the reaction is normally carried out under reflux conditions in 60% ethanol:, Wiley-VCH p 499
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Experimentally, the reaction is normally carried out under reflux conditions in 60% ethanol:. Becker H.G., Berger W., Domschke G., Fanghänel E., Faust J., Fischer M., Gentz F., Gewald K., Gluch R., Mayer R., Müller K., Pavel D., Schmidt H., Schollberg K., Schwetlick K., Seiler E., and Zeppenfeld G. Organikum (1999), Wiley-VCH p 499
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Faust, J.5
Fischer, M.6
Gentz, F.7
Gewald, K.8
Gluch, R.9
Mayer, R.10
Müller, K.11
Pavel, D.12
Schmidt, H.13
Schollberg, K.14
Schwetlick, K.15
Seiler, E.16
Zeppenfeld, G.17
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45
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Frisch M.J., Trucks G.W., Schlegel H.B., Scuseria G.E., Robb M.A., Cheeseman J.R., Montgomery Jr. J.A., Vreven T., Kudin K.N., Burant J.C., Millam J.M., Iyengar S.S., Tomasi J., Barone V., Mennucci B., Cossi M., Scalmani G., Rega N., Petersson G.A., Nakatsuji H., Hada M., Ehara M., Toyota K., Fukuda R., Hasegawa J., Ishida M., Nakajima T., Honda Y., Kitao O., Nakai H., Klene M., Li X., Knox J.E., Hratchian H.P., Cross J.B., Adamo C., Jaramillo J., Gomperts R., Stratmann R.E., Yazyev O., Austin A.J., Cammi R., Pomelli C., Ochterski J.W., Ayala P.Y., Morokuma K., Voth G.A., Salvador P., Dannenberg J.J., Zakrzewski V.G., Dapprich S., Daniels A.D., Strain M.C., Farkas O., Malick D.K., Rabuck A.D., Raghavachari K., Foresman J.B., Ortiz J.V., Cui Q., Baboul A.G., Clifford S., Cioslowski J., Stefanov B.B., Liu G., Liashenko A., Piskorz P., Komaromi I., Martin R.L., Fox D.J., Keith T., Al-Laham M.A., Peng C.Y., Nanayakkara A., Challacombe M., Gill P.M.W., Johnson B., Chen W., Wong M.W., Gonzalez C., and Pople J.A. Gaussian 03, Revision C.02 (2004), Gaussian, Wallingford, CT
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(2004)
Gaussian 03, Revision C.02
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Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
Montgomery Jr., J.A.7
Vreven, T.8
Kudin, K.N.9
Burant, J.C.10
Millam, J.M.11
Iyengar, S.S.12
Tomasi, J.13
Barone, V.14
Mennucci, B.15
Cossi, M.16
Scalmani, G.17
Rega, N.18
Petersson, G.A.19
Nakatsuji, H.20
Hada, M.21
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
Ochterski, J.W.44
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
Gill, P.M.W.76
Johnson, B.77
Chen, W.78
Wong, M.W.79
Gonzalez, C.80
Pople, J.A.81
more..
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46
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Implementation:
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Becke, A.D.1
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