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8
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77951084072
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For a computational analysis of diterpene biosynthetic pathways see: (b)
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For a computational analysis of diterpene biosynthetic pathways see: (b) Y.J. Hong, and D.J. Tantillo J. Am. Chem. Soc. 132 2010 5375
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Hong, Y.J.1
Tantillo, D.J.2
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84929949390
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Several nitrogen sources (e.g., methylamine, ethylamine, β-aminoethanol and S-adenosylmethionine) have been proposed as precursors to the nitrogen atom found in the diterpene alkaloids (see Ref. 6c, p 87). However, to date, only l-serine has been identified as a nitrogen source, see Ref. 6b
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Several nitrogen sources (e.g., methylamine, ethylamine, β-aminoethanol and S-adenosylmethionine) have been proposed as precursors to the nitrogen atom found in the diterpene alkaloids (see Ref. 6c, p 87). However, to date, only l-serine has been identified as a nitrogen source, see Ref. 6b.
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13
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65649106629
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P.-J. Zhao, S. Gao, L.-M. Fan, J.-L. Nie, H.-P. He, Y. Zeng, Y.-M. Shen, and X.-J. Hao J. Nat. Prod. 72 2009 645
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Zeng, Y.6
Shen, Y.-M.7
Hao, X.-J.8
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16
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84929947459
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Previously Wang and Liang classified the arcutines as a rearranged class (C-II′) of the hetidines or hetisines, see Ref. 6c
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Previously Wang and Liang classified the arcutines as a rearranged class (C-II′) of the hetidines or hetisines, see Ref. 6c.
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17
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80052174614
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The overall transformation could also occur in a dyotropic manner, see, for example
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The overall transformation could also occur in a dyotropic manner, see, for example, R.L. Davis, C.A. Leverett, D. Romo, and D.J. Tantillo J. Org. Chem. 76 2011 7167
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Davis, R.L.1
Leverett, C.A.2
Romo, D.3
Tantillo, D.J.4
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Université de Sherbrooke ()
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C.Y. Legault CYLview, 1.0b 2009 Université de Sherbrooke (http://www.cylview.org)
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CYLview, 1.0b
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Legault, C.Y.1
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Gaussian 09, Revision C.01 Gaussian Wallingford CT
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M.J. Frisch, G.W. Trucks, H.B. Schlegel, G.E. Scuseria, M.A. Robb, J.R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, G.A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H.P. Hratchian, A.F. Izmaylov, J. Bloino, G. Zheng, J.L. Sonnenberg, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, T. Vreven, J.A. Montgomery Jr., J.E. Peralta, F. Ogliaro, M. Bearpark, J.J. Heyd, E. Brothers, K.N. Kudin, V.N. Staroverov, R. Kobayashi, J. Normand, K. Raghavachari, A. Rendell, J.C. Burant, S.S. Iyengar, J. Tomasi, M. Cossi, N. Rega, J.M. Millam, M. Klene, J.E. Knox, J.B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R.E. Stratmann, O. Yazyev, A.J. Austin, R. Cammi, C. Pomelli, J.W. Ochterski, R.L. Martin, K. Morokuma, V.G. Zakrzewski, G.A. Voth, P. Salvador, J.J. Dannenberg, S. Dapprich, A.D. Daniels, Ö. Farkas, J.B. Foresman, J.V. Ortiz, J. Cioslowski, and D.J. Fox Gaussian 09, Revision C.01 2009 Gaussian Wallingford CT
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(2009)
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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
Scalmani, G.7
Barone, V.8
Mennucci, B.9
Petersson, G.A.10
Nakatsuji, H.11
Caricato, M.12
Li, X.13
Hratchian, H.P.14
Izmaylov, A.F.15
Bloino, J.16
Zheng, G.17
Sonnenberg, J.L.18
Hada, M.19
Ehara, M.20
Toyota, K.21
Fukuda, R.22
Hasegawa, J.23
Ishida, M.24
Nakajima, T.25
Honda, Y.26
Kitao, O.27
Nakai, H.28
Vreven, T.29
Montgomery, Jr.J.A.30
Peralta, J.E.31
Ogliaro, F.32
Bearpark, M.33
Heyd, J.J.34
Brothers, E.35
Kudin, K.N.36
Staroverov, V.N.37
Kobayashi, R.38
Normand, J.39
Raghavachari, K.40
Rendell, A.41
Burant, J.C.42
Iyengar, S.S.43
Tomasi, J.44
Cossi, M.45
Rega, N.46
Millam, J.M.47
Klene, M.48
Knox, J.E.49
Cross, J.B.50
Bakken, V.51
Adamo, C.52
Jaramillo, J.53
Gomperts, R.54
Stratmann, R.E.55
Yazyev, O.56
Austin, A.J.57
Cammi, R.58
Pomelli, C.59
Ochterski, J.W.60
Martin, R.L.61
Morokuma, K.62
Zakrzewski, V.G.63
Voth, G.A.64
Salvador, P.65
Dannenberg, J.J.66
Dapprich, S.67
Daniels, A.D.68
Farkas Ö.69
Foresman, J.B.70
Ortiz, J.V.71
Cioslowski, J.72
Fox, D.J.73
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Data included in Supporting information
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Data included in Supporting information.
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