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Heliannuols A and K: for racemic syntheses, see: F. Lecornué, and J. Ollivier Synlett 2004 1613 1615
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JP06128238 [C. A., 1995, 123, 55900].
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Kaiho, T.; Yokoyama, T.; Mori, H.; Fujiwara, J.; Nobori, T.; Okada, H.; Kamiya, J.; Maruyama, M.; Sugawara, T. JP06128238, 1994; [C. A., 1995, 123, 55900].
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Mori, H.3
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Nobori, T.5
Okada, H.6
Kamiya, J.7
Maruyama, M.8
Sugawara, T.9
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21
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0001686113
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For examples of the construction of a tertiary stereogenic center at the benzylic position by chirality transfer during the aromatic Claisen rearrangement, see: H.L. Goerring, and W.I. Kimoto J. Am. Chem. Soc. 87 1965 1748 1753
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von J. Borgulya, R. Madeja, P. Fahrni, H.-J. Hansen, H. Schmid, and R. Barner Helv. Chim. Acta 56 1973 14 75
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Castro, A.M.M.1
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38
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79958176553
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Since we were not able to obtain the sample of natural heliannuol K, the discrepancy with the optical rotation of synthetic product with that reported for the natural product could not be explained
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Since we were not able to obtain the sample of natural heliannuol K, the discrepancy with the optical rotation of synthetic product with that reported for the natural product could not be explained.
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39
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79958111008
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Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Center as supplementary publication number CCDC 816717. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: +44 1223 336033 or e-mail: deposit@ccdc.cam.ac.uk]
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Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Center as supplementary publication number CCDC 816717. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK [fax: +44 1223 336033 or e-mail: deposit@ccdc.cam.ac.uk ].
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