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Coppola, G.M.; Schuster, H.F. Asymmetric Synthesis, Construction of Chiral Molecules Using Amino Acids, John Wiley & Sons, 1987; Scott, J.W. Asymmetric Synthesis, Morrison, J.D.; Scott, J.W. ed., Academic Press, 1984, vol. 4, pp 1-226; Inch, T.D. Tetrahedron 1984, 40, 3161-3213; Hanessian, S. Total Synthesis of Natural Products: The Chiron Approach, Pergamon Press, 1983.
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Morrison, J.D.; Scott, J.W. ed., Academic Press
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Coppola, G.M.; Schuster, H.F. Asymmetric Synthesis, Construction of Chiral Molecules Using Amino Acids, John Wiley & Sons, 1987; Scott, J.W. Asymmetric Synthesis, Morrison, J.D.; Scott, J.W. ed., Academic Press, 1984, vol. 4, pp 1-226; Inch, T.D. Tetrahedron 1984, 40, 3161-3213; Hanessian, S. Total Synthesis of Natural Products: The Chiron Approach, Pergamon Press, 1983.
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Scott, J.W.1
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Coppola, G.M.; Schuster, H.F. Asymmetric Synthesis, Construction of Chiral Molecules Using Amino Acids, John Wiley & Sons, 1987; Scott, J.W. Asymmetric Synthesis, Morrison, J.D.; Scott, J.W. ed., Academic Press, 1984, vol. 4, pp 1-226; Inch, T.D. Tetrahedron 1984, 40, 3161-3213; Hanessian, S. Total Synthesis of Natural Products: The Chiron Approach, Pergamon Press, 1983.
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Coppola, G.M.; Schuster, H.F. Asymmetric Synthesis, Construction of Chiral Molecules Using Amino Acids, John Wiley & Sons, 1987; Scott, J.W. Asymmetric Synthesis, Morrison, J.D.; Scott, J.W. ed., Academic Press, 1984, vol. 4, pp 1-226; Inch, T.D. Tetrahedron 1984, 40, 3161-3213; Hanessian, S. Total Synthesis of Natural Products: The Chiron Approach, Pergamon Press, 1983.
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a. Colegate, S.M.; Aust. J. Chem. 1979, 32, 2257-2264; Mubarak, A.M.; Brown, D.C. J. Chem. Soc., Perkin 1 1982, 809-813; Machinaga, N.; Kibayashi, C. J. Org. Chem. 1991, 56, 1386-1393; Marzi, M; Minetti, P.; Misiti, D. Tetrahedron 1992, 46, 10127-10132; Fitremann, J.; Dureault, A.; Depezay, J-C. Tetrahedron 1995, 51, 9581-9594.
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Minetti, P.2
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a. Colegate, S.M.; Aust. J. Chem. 1979, 32, 2257-2264; Mubarak, A.M.; Brown, D.C. J. Chem. Soc., Perkin 1 1982, 809-813; Machinaga, N.; Kibayashi, C. J. Org. Chem. 1991, 56, 1386-1393; Marzi, M; Minetti, P.; Misiti, D. Tetrahedron 1992, 46, 10127-10132; Fitremann, J.; Dureault, A.; Depezay, J-C. Tetrahedron 1995, 51, 9581-9594.
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Depezay, J.-C.2
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b. Jurczak, J.; Pikul, S.; Bauer, T. Tetrahedron 1986, 42, 447-448, and the references cited therein; Takano, S.; Kurotani, A.; Ogasawara, K. Synthesis 1987, 1075-1078; Peters, U.; Bankova, W.; Welzel, P. Tetrahedron 1987, 43, 3803-3816; Krief, A.; Dumont, W.; Lecomte, P. Tetrahedron 1989, 45, 3039-3052.
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b. Jurczak, J.; Pikul, S.; Bauer, T. Tetrahedron 1986, 42, 447-448, and the references cited therein; Takano, S.; Kurotani, A.; Ogasawara, K. Synthesis 1987, 1075-1078; Peters, U.; Bankova, W.; Welzel, P. Tetrahedron 1987, 43, 3803-3816; Krief, A.; Dumont, W.; Lecomte, P. Tetrahedron 1989, 45, 3039-3052.
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Takano, S.1
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b. Jurczak, J.; Pikul, S.; Bauer, T. Tetrahedron 1986, 42, 447-448, and the references cited therein; Takano, S.; Kurotani, A.; Ogasawara, K. Synthesis 1987, 1075-1078; Peters, U.; Bankova, W.; Welzel, P. Tetrahedron 1987, 43, 3803-3816; Krief, A.; Dumont, W.; Lecomte, P. Tetrahedron 1989, 45, 3039-3052.
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b. Jurczak, J.; Pikul, S.; Bauer, T. Tetrahedron 1986, 42, 447-448, and the references cited therein; Takano, S.; Kurotani, A.; Ogasawara, K. Synthesis 1987, 1075-1078; Peters, U.; Bankova, W.; Welzel, P. Tetrahedron 1987, 43, 3803-3816; Krief, A.; Dumont, W.; Lecomte, P. Tetrahedron 1989, 45, 3039-3052.
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c. Kotsuki, H.; Nishikawa, H.; Mori, Y.; Ochi, M. J. Org. Chem. 1992, 57, 5036-5040.
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a. For review: Elix, J.A.; Whitton, A.A. Progress in the Chemistry of Organic Natural Products, Springer-Verlag, 1984, vol. 45, pp 103-234. For the isolation and the structural determination: Chester, D.O.; Elix, J.A. Aust. J. Chem. 1979, 32, 2565-2569, and references cited therein. For the latest chiral synthesis: Martin, T.; Rodriguez, C.M.; Martin, V.S. J. Org. Chem. 1996, 61, 6450-6453.
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a. For review: Elix, J.A.; Whitton, A.A. Progress in the Chemistry of Organic Natural Products, Springer-Verlag, 1984, vol. 45, pp 103-234. For the isolation and the structural determination: Chester, D.O.; Elix, J.A. Aust. J. Chem. 1979, 32, 2565-2569, and references cited therein. For the latest chiral synthesis: Martin, T.; Rodriguez, C.M.; Martin, V.S. J. Org. Chem. 1996, 61, 6450-6453.
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Chester, D.O.1
Elix, J.A.2
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0029789618
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a. For review: Elix, J.A.; Whitton, A.A. Progress in the Chemistry of Organic Natural Products, Springer-Verlag, 1984, vol. 45, pp 103-234. For the isolation and the structural determination: Chester, D.O.; Elix, J.A. Aust. J. Chem. 1979, 32, 2565-2569, and references cited therein. For the latest chiral synthesis: Martin, T.; Rodriguez, C.M.; Martin, V.S. J. Org. Chem. 1996, 61, 6450-6453.
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Martin, T.1
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Martin, V.S.3
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84941381436
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and references cited therein. For the latest chiral synthesis: the literature cited in the same item of ref. 3a
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b. For the isolation: Huneck, S.; Follmann, G.Z. Naturforsch. B 1967, 22, 666-670, and references cited therein. For the latest chiral synthesis: the literature cited in the same item of ref. 3a.
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Naturforsch. B
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Huneck, S.1
Follmann, G.Z.2
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0023897844
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c. For the isolation: Park, B.K.; Nagasawa, M.; Hirota, A.; Nakayama, M. J. Antibiot. 1988, 41, 751-758. For the latest chiral synthesis: Vaupel, A.; Knochel, P. J. Org. Chem., 1996, 61, 5743-5753.
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J. Antibiot.
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0000631827
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c. For the isolation: Park, B.K.; Nagasawa, M.; Hirota, A.; Nakayama, M. J. Antibiot. 1988, 41, 751-758. For the latest chiral synthesis: Vaupel, A.; Knochel, P. J. Org. Chem., 1996, 61, 5743-5753.
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J. Org. Chem.
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Felix, D.; Gschwend-Steen, K.; Wick, A.E.; Eschenmoser, A. Helv. Chim. Acta 1969, 52, 1030-1042; Corey, E.J.; Shibasaki, M.; Knolle, J. Tetrahedron Lett. 1977, 1625-1626.
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Felix, D.; Gschwend-Steen, K.; Wick, A.E.; Eschenmoser, A. Helv. Chim. Acta 1969, 52, 1030-1042; Corey, E.J.; Shibasaki, M.; Knolle, J. Tetrahedron Lett. 1977, 1625-1626.
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0001691559
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Morpain, C.; Nasser, B.; Laude, B.; Latruffe, N. Org. Prep. Proced. Intern. 1990, 22, 540-543; Eastwood, F.W.; Harrington, K.J.; Josan, J.S.; Pura, J.L. Tetrahedron Lett. 1970, 11, 5223-5224.
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25
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0013595685
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note
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w=0.060.
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26
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0000994397
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2CuLi) than direct alkylation of β-methyl- γ -tosyloxymethyl- γ -lactone to obtain trans-whisky lactone and the congeners: Ebata, T.; Matsumoto, K.; Yoshikoshi, H.; Koseki, K.; Kawakami, H.; Okano, K.; Matsushita, H. Heterocycles 1993, 36, 1017-1026.
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Ebata, T.1
Matsumoto, K.2
Yoshikoshi, H.3
Koseki, K.4
Kawakami, H.5
Okano, K.6
Matsushita, H.7
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0026782629
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a. de Azevedo, M.B.M; Murta, M.M.; Greene, A.E. J. Org. Chem. 1992, 57, 4567-4569.
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De Azevedo, M.B.M.1
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Greene, A.E.3
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0027749503
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b. Murta, M.M.; de Azevedo, M.B.M.; Greene, A.E. J. Org. Chem. 1993, 58, 7537-7541.
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Murta, M.M.1
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