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1
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38949180620
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and previous articles in this series
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J.W. Blunt, B. R. Copp, W.-P. Hu, M. H. G. Mimro, P. T. Northcote, M. R. Prinsep, Nat. Prod. Rep. 2008, 25,35-94, and previous articles in this series.
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Copp, B.R.2
Hu, W.-P.3
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Northcote, P.T.5
Prinsep, M.R.6
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5
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34247550727
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A. M. S. Mayer, A. D. Rodríguez, R. G. S. Berlinck, M. T. Hamann, Comp. Biochem. Physiol. Part C 2007, 145, 553-581.
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Comp. Biochem. Physiol. Part C
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Mayer, A.M.S.1
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Berlinck, R.G.S.3
Hamann, M.T.4
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6
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33645968948
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a) C. Duque, M. Puyana, L. Castellanos, A. Arias, H. Correa, O. Osorno, T. Asai, N. Hara, Y. Fujimoto, Tetrahedron 2006, 62, 4205-4213;
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Tetrahedron
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Puyana, M.2
Castellanos, L.3
Arias, A.4
Correa, H.5
Osorno, O.6
Asai, T.7
Hara, N.8
Fujimoto, Y.9
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b) A. D. Rodríguez, C. Ramírez, I.I. Rodríguez, E. González, Org. Lett. 1999, 1, 527-530;
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e) A. Ata, R. G. Kerr, C. E. Moya, R. S. Jacobs, Tetrahedron 2003, 59, 4215-4222.
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16
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60849128065
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Eds, J. S. Splitter, F. Turecek, VCH Publishers, Inc, New York, chapter 6
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F. Turecek, in Applications of Mass Spectrometry to Organic Stereochemistry (Eds.: J. S. Splitter, F. Turecek), VCH Publishers, Inc., New York, 1994, chapter 6.
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Applications of Mass Spectrometry to Organic Stereochemistry
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Turecek, F.1
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0032476081
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A. D. Rodríguez, E. González, S. D. Huang, J. Org. Chem. 1998, 63, 7083-7091.
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Rodríguez, A.D.1
González, E.2
Huang, S.D.3
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18
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0033595863
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3 solution were used to establish the structural (and stereochemical) relatedness of compounds 5 and 11. For the structural elucidation work on sandresolide B (11), see: A. D. Rodríguez, C. Ramírez, I. I. Rodríguez, Tetrahedron Lett. 1999, 40, 7627-7631.
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3 solution were used to establish the structural (and stereochemical) relatedness of compounds 5 and 11. For the structural elucidation work on sandresolide B (11), see: A. D. Rodríguez, C. Ramírez, I. I. Rodríguez, Tetrahedron Lett. 1999, 40, 7627-7631.
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19
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60849116848
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The McSpartan '04 molecular modeling program was used to calculate the conformer distribution of each possible structure. Key interproton distances were then measured on the lowest-energy conformer. These distances are shown in Figure 2 together with selected observed NOESY correlations.
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The McSpartan '04 molecular modeling program was used to calculate the conformer distribution of each possible structure. Key interproton distances were then measured on the lowest-energy conformer. These distances are shown in Figure 2 together with selected observed NOESY correlations.
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20
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84868891574
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3OD (without a trace of acid or base catalyst) was achieved slowly after heating of sandresolide C (5)at55 °Cfor 4-5 days. LREIMS analysis of the product obtained revealed a molecular ion species at m/z =321.
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3OD (without a trace of acid or base catalyst) was achieved slowly after heating of sandresolide C (5)at55 °Cfor 4-5 days. LREIMS analysis of the product obtained revealed a molecular ion species at m/z =321.
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21
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0003539011
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VCH Publishers, Inc, New York, chapter 5
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K. Pihlaja, E. Kleinpeter, Carbon-13 NMR Chemical shift in Structural and Stereochemical analysis, VCH Publishers, Inc., New York, 1994, chapter 5.
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Carbon-13 NMR Chemical shift in Structural and Stereochemical analysis
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Pihlaja, K.1
Kleinpeter, E.2
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22
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84868911372
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C=O = 204.9 ppm).
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C=O = 204.9 ppm).
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23
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34548732383
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In addition to a plethora of C20-rearranged diterpenes, other classes of C19, C18, C17, and C 16-rearranged terpenoids have been isolated from P. elisabethae; see: a X. Wei, 1.1. Rodríguez, A. D. Rodríguez, C. L. Barnes, J. Org. Chem. 2007, 72, 7386-7389;
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16-rearranged terpenoids have been isolated from P. elisabethae; see: a) X. Wei, 1.1. Rodríguez, A. D. Rodríguez, C. L. Barnes, J. Org. Chem. 2007, 72, 7386-7389;
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24
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0142181704
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b) A. D. Rodríguez, C. Ramírez, V. Medina, Y.-P. Shi, Tetrahedron Lett. 2000, 41, 5177-5180;
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Tetrahedron Lett
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Rodríguez, A.D.1
Ramírez, C.2
Medina, V.3
Shi, Y.-P.4
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27
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0033090669
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A. M. S. Mayer, S. Oh, K. H. Ramsey, P. B. Jacobson, K. B. Glaser, A. M. Romanic, Shock 1999, 11, 180-186.
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7044264517
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I.I. Rodríguez, Y.-P. Shi, O.J. García, A. D. Rodríguez, A. M. S. Mayer, J. A. Sánchez, E. Ortega-Barria, J. González, J. Nat. Prod. 2004, 67, 1672-1680.
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0025775062
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