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For a recent review see: Ward, R. S., Asymmetric synthesis of lignans. Tetrahedron, 46, 5029-5041 (1990).
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Tetrahedron
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Ward, R.S.1
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Biological activities of lignans
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For a review see: MacRae, W. D. and Towers, G. H. N., Biological activities of lignans. Phytochemistry, 23, 1207-1220 (1984); MacRae, W. D., Hudson, J. B., and Towers, G. H. N., The antiviral action of lignans. Planta Medica, 55, 531-535 (1989).
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Phytochemistry
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MacRae, W.D.1
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For a review see: MacRae, W. D. and Towers, G. H. N., Biological activities of lignans. Phytochemistry, 23, 1207-1220 (1984); MacRae, W. D., Hudson, J. B., and Towers, G. H. N., The antiviral action of lignans. Planta Medica, 55, 531-535 (1989).
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MacRae, W.D.1
Hudson, J.B.2
Towers, G.H.N.3
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0023851254
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Enantio-controlled route to the furofuran lignans: The total synthesis of (-)-sesamolin, (-)-sesamine, and (-)-acuminatolide
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For example: Takano, S., Ohkawa, T., Tamori, S., Satoh, S., and Ogasawara, K., Enantio-controlled route to the furofuran lignans: The total synthesis of (-)-sesamolin, (-)-sesamine, and (-)-acuminatolide. J. Chem. Soc., Chem. Commun., 189-191 (1989); Pelter, A., Ward, R. S., and Little, G. M., Approaches to 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane lignans via asymmetric synthesis of dihydro-and tetrahydro-furan derivatives. J. Chem. Soc., Perkin Trans. I, 277-2790 (1990); Yoshida, S., Yamanaka, T., Miyake, T., Moritani, Y., Ohmizu, H., and Iwasaki, T., A novel asymmetric synthesis of axial-equatorial furofuran lignans: A synthesis of (+)-fargesin. Tetrahedron Lett., 36, 7271-7274 (1995); Van Oeveren, A., Jansen, J. F. G. A., and Feringa, B. L., Enantioselective synthesis of natural dibenzyl-butyrolactone lignans (-)-enterolactone, (-)-hinokinin, (-)-pluviatolide, (-)-enterodiol, and furofuran lignan (-)-eudesmin via tandem conjugate addition to γ-alkoxybutenolides. J. Org. Chem., 59, 5999-6007 (1994); Wirth, T., First total synthesis of (+)-membrine. Libigs Ann./Recueil, 1155-1158 (1997).
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Takano, S.1
Ohkawa, T.2
Tamori, S.3
Satoh, S.4
Ogasawara, K.5
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5
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37049084345
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Approaches to 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane lignans via asymmetric synthesis of dihydro-and tetrahydro-furan derivatives
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For example: Takano, S., Ohkawa, T., Tamori, S., Satoh, S., and Ogasawara, K., Enantio-controlled route to the furofuran lignans: The total synthesis of (-)-sesamolin, (-)-sesamine, and (-)-acuminatolide. J. Chem. Soc., Chem. Commun., 189-191 (1989); Pelter, A., Ward, R. S., and Little, G. M., Approaches to 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane lignans via asymmetric synthesis of dihydro-and tetrahydro-furan derivatives. J. Chem. Soc., Perkin Trans. I, 277-2790 (1990); Yoshida, S., Yamanaka, T., Miyake, T., Moritani, Y., Ohmizu, H., and Iwasaki, T., A novel asymmetric synthesis of axial-equatorial furofuran lignans: A synthesis of (+)-fargesin. Tetrahedron Lett., 36, 7271-7274 (1995); Van Oeveren, A., Jansen, J. F. G. A., and Feringa, B. L., Enantioselective synthesis of natural dibenzyl-butyrolactone lignans (-)-enterolactone, (-)-hinokinin, (-)-pluviatolide, (-)-enterodiol, and furofuran lignan (-)-eudesmin via tandem conjugate addition to γ-alkoxybutenolides. J. Org. Chem., 59, 5999-6007 (1994); Wirth, T., First total synthesis of (+)-membrine. Libigs Ann./Recueil, 1155-1158 (1997).
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J. Chem. Soc., Perkin Trans. I
, pp. 277-2790
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Pelter, A.1
Ward, R.S.2
Little, G.M.3
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A novel asymmetric synthesis of axial-equatorial furofuran lignans: A synthesis of (+)-fargesin
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For example: Takano, S., Ohkawa, T., Tamori, S., Satoh, S., and Ogasawara, K., Enantio-controlled route to the furofuran lignans: The total synthesis of (-)-sesamolin, (-)-sesamine, and (-)-acuminatolide. J. Chem. Soc., Chem. Commun., 189-191 (1989); Pelter, A., Ward, R. S., and Little, G. M., Approaches to 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane lignans via asymmetric synthesis of dihydro-and tetrahydro-furan derivatives. J. Chem. Soc., Perkin Trans. I, 277-2790 (1990); Yoshida, S., Yamanaka, T., Miyake, T., Moritani, Y., Ohmizu, H., and Iwasaki, T., A novel asymmetric synthesis of axial-equatorial furofuran lignans: A synthesis of (+)-fargesin. Tetrahedron Lett., 36, 7271-7274 (1995); Van Oeveren, A., Jansen, J. F. G. A., and Feringa, B. L., Enantioselective synthesis of natural dibenzyl-butyrolactone lignans (-)-enterolactone, (-)-hinokinin, (-)-pluviatolide, (-)-enterodiol, and furofuran lignan (-)-eudesmin via tandem conjugate addition to γ-alkoxybutenolides. J. Org. Chem., 59, 5999-6007 (1994); Wirth, T., First total synthesis of (+)-membrine. Libigs Ann./Recueil, 1155-1158 (1997).
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Tetrahedron Lett.
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Yoshida, S.1
Yamanaka, T.2
Miyake, T.3
Moritani, Y.4
Ohmizu, H.5
Iwasaki, T.6
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7
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0028127282
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Enantioselective synthesis of natural dibenzyl-butyrolactone lignans (-)-enterolactone, (-)-hinokinin, (-)-pluviatolide, (-)-enterodiol, and furofuran lignan (-)-eudesmin via tandem conjugate addition to γ-alkoxybutenolides
-
For example: Takano, S., Ohkawa, T., Tamori, S., Satoh, S., and Ogasawara, K., Enantio-controlled route to the furofuran lignans: The total synthesis of (-)-sesamolin, (-)-sesamine, and (-)-acuminatolide. J. Chem. Soc., Chem. Commun., 189-191 (1989); Pelter, A., Ward, R. S., and Little, G. M., Approaches to 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane lignans via asymmetric synthesis of dihydro-and tetrahydro-furan derivatives. J. Chem. Soc., Perkin Trans. I, 277-2790 (1990); Yoshida, S., Yamanaka, T., Miyake, T., Moritani, Y., Ohmizu, H., and Iwasaki, T., A novel asymmetric synthesis of axial-equatorial furofuran lignans: A synthesis of (+)-fargesin. Tetrahedron Lett., 36, 7271-7274 (1995); Van Oeveren, A., Jansen, J. F. G. A., and Feringa, B. L., Enantioselective synthesis of natural dibenzyl-butyrolactone lignans (-)-enterolactone, (-)-hinokinin, (-)-pluviatolide, (-)-enterodiol, and furofuran lignan (-)-eudesmin via tandem conjugate addition to γ-alkoxybutenolides. J. Org. Chem., 59, 5999-6007 (1994); Wirth, T., First total synthesis of (+)-membrine. Libigs Ann./Recueil, 1155-1158 (1997).
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Van Oeveren, A.1
Jansen, J.F.G.A.2
Feringa, B.L.3
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First total synthesis of (+)-membrine
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For example: Takano, S., Ohkawa, T., Tamori, S., Satoh, S., and Ogasawara, K., Enantio-controlled route to the furofuran lignans: The total synthesis of (-)-sesamolin, (-)-sesamine, and (-)-acuminatolide. J. Chem. Soc., Chem. Commun., 189-191 (1989); Pelter, A., Ward, R. S., and Little, G. M., Approaches to 2,6-diaryl-3,7-dioxabicyclo[3.3.0]octane lignans via asymmetric synthesis of dihydro-and tetrahydro-furan derivatives. J. Chem. Soc., Perkin Trans. I, 277-2790 (1990); Yoshida, S., Yamanaka, T., Miyake, T., Moritani, Y., Ohmizu, H., and Iwasaki, T., A novel asymmetric synthesis of axial-equatorial furofuran lignans: A synthesis of (+)-fargesin. Tetrahedron Lett., 36, 7271-7274 (1995); Van Oeveren, A., Jansen, J. F. G. A., and Feringa, B. L., Enantioselective synthesis of natural dibenzyl-butyrolactone lignans (-)-enterolactone, (-)-hinokinin, (-)-pluviatolide, (-)-enterodiol, and furofuran lignan (-)-eudesmin via tandem conjugate addition to γ-alkoxybutenolides. J. Org. Chem., 59, 5999-6007 (1994); Wirth, T., First total synthesis of (+)-membrine. Libigs Ann./Recueil, 1155-1158 (1997).
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Libigs Ann./Recueil
, pp. 1155-1158
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Wirth, T.1
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9
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Total synthesis of (+)-paulownin
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Okazaki, M., Ishibashi, F., Shuto, Y., and Taniguchi, E., Total synthesis of (+)-paulownin. Biosci. Biotechnol. Biochem., 61, 743-745 (1997).
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A total synthesis of racemic paulownin using a type II photocyclization reaction
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Kraus, G. A. and Chen, L., A total synthesis of racemic paulownin using a type II photocyclization reaction. J. Am. Chem. Soc., 112, 3464-3466 (1990).
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Total synthesis of (+)-phrymarolin I from (+)-malic acid
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Okaszaki, M., Ishibashi, F., Shuto, Y., and Taniguchi, E., Total synthesis of (+)-phrymarolin I from (+)-malic Acid. Biosci. Biotechnol. Biochem., 61, 660-663 (1997).
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Combination of borane-dimethylsulfide complex with catalytic sodium tetrahydroborate as a selective reducing agent for α-hydroxy esters. Versatile chiral building block from (S)-(-)-malic acid
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Saito, S., Hasegawa, T., Inaba, M., Nishida, R., Fujii, T., Nomizu, S., and Moriwake, T., Combination of borane-dimethylsulfide complex with catalytic sodium tetrahydroborate as a selective reducing agent for α-hydroxy esters. Versatile chiral building block from (S)-(-)-malic acid. Chem. Lett., 1389-1392 (1984).
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