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1
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0026648309
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Isolation of sphingofungins A-D: (a) VanMiddlesworth F., Giacobbe R.A., Lopez M., Garrity G., Bland J.A., Bartizal K., Fromtling R.A., Polishook J., Zweerink M., Edison A.M., Rozdilsky W., Wilson K.E., Monaghan R.A. J. Antibiot. 45:1992;861-867.
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VanMiddlesworth, F.1
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Bland, J.A.5
Bartizal, K.6
Fromtling, R.A.7
Polishook, J.8
Zweerink, M.9
Edison, A.M.10
Rozdilsky, W.11
Wilson, K.E.12
Monaghan, R.A.13
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2
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0026570297
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Structure elucidation: (b) VanMiddlesworth F., Dufresne C., Wincott F.E., Mosley R.T., Wilson K.E. Tetrahedron Lett. 33:1992;297-300.
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Mosley, R.T.4
Wilson, K.E.5
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3
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0026499739
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Isolation of sphingofungins E and F: (c) Horn W.S., Smith T.L., Bills G.F., Raghoobar S.L., Helms G.L., Kurts M.B., Marrinan J.A., Frommer B.R., Thornton R.A., Mandara S.M. J. Antibiot. 45:1992;1692-1696.
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Horn, W.S.1
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Helms, G.L.5
Kurts, M.B.6
Marrinan, J.A.7
Frommer, B.R.8
Thornton, R.A.9
Mandara, S.M.10
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4
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(a) Fujita T., Inoue K., Yamamoto S., Ikumoto T., Sasaki S., Toyama R., Yoneta M., Hoshino Y., Okumoto T. J. Antibiot. 47:1994;208.
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Fujita, T.1
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Toyama, R.6
Yoneta, M.7
Hoshino, Y.8
Okumoto, T.9
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(b) Miyake Y., Kozutsumi Y., Nakamura S., Fujita T., Kawasaki T. Biochem. Biophys. Res. Commun. 211:1995;396.
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Kawasaki, T.5
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6
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0020422494
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For total syntheses of myriocin, see: (a) Banfi L., Bretta M.G., Colombo L., Gennari C., Scolastico C. J. Chem. Soc., Chem. Commun. 1982;488.
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Banfi, L.1
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Gennari, C.4
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(b) Banfi L., Bretta M.G., Colombo L., Gennari C., Scolastico C. J. Chem. Soc., Perkin Trans. 1. 1983;1613.
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Banfi, L.1
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Colombo, L.3
Gennari, C.4
Scolastico, C.5
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(e) Sano S., Kobayashi Y., Kondo T., Takebayashi M., Maruyama S., Fujita T., Nagano Y. Tetrahedron Lett. 36:1995;2097.
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Fujita, T.6
Nagano, Y.7
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(f) Hatakeyama S., Yoshida M., Esumi T., Iwabuchi Y., Irie H., Kawamoto T., Yamada H., Nishizawa M. Tetrahedron Lett. 45:1997;7887.
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Irie, H.5
Kawamoto, T.6
Yamada, H.7
Nishizawa, M.8
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12
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0029017178
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For total synthesis of sphingofungin D, see: (a) Chida N., Ikemoto H., Noguchi A., Amano S., Ogawa S. Nat. Prod. Lett. 6:1995;295.
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(d) Kobayashi S., Matsumura M., Furuta T., Hayashi T., Iwamoto S. Synlett. 1997;301.
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Kobayashi, S.1
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16
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see also 4256
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(e) Kobayashi S., Furuta T., Hayashi T., Nishijima M., Hanada K. J. Am. Chem. Soc. 120:1998;908-919, see also 4256.
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Kobayashi, S.1
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(d) Oishi T., Ando K., Inomiya K., Sato H., Iida M., Chida N. Org. Lett. 4:2002;151-154.
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Sato, H.4
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0032527965
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For total synthesis of sphingofungin F, see: Ref. 2c, (a) Trost B.M., Lee C.B. J. Am. Chem. Soc. 120:1998;6818-6819.
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Trost, B.M.1
Lee, C.B.2
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24
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(a) Miyaura N., Ishiyama T., Sasaki H., Ishikawa M., Satoh M., Suzuki A. J. Am. Chem. Soc. 111:1989;314-321.
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For a recent review on the B-alkyl Suzuki-Miyaura cross-coupling reaction, see: (b) Miyaura N., Suzuki A. Chem. Rev. 95:1995;2457.
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(a) Sato K., Suzuki K., Ueda M., Katayama M., Kajihara Y. Chem. Lett. 1991;1469-1472.
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S. Hanessian. New York: Marcel Dekker
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For a review on the synthesis of branched-chain sugars, see: (b) Hanessian S., Preparative Carbohydrate Chemistry. 1997;207-262 Marcel Dekker, New York.
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32
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0011243429
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α-Chloroepoxide 12 was obtained as a single diastereomer. The stereochemistry of the newly formed chiral center (α-position of the chloride) was not determined
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α-Chloroepoxide 12 was obtained as a single diastereomer. The stereochemistry of the newly formed chiral center (α-position of the chloride) was not determined.
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36
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0011231814
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