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(a) Tezuka, Y.; Ali, M. S.; Banskota, A. H.; Kadota, S. Tetrahedron Lett. 2000, 41, 5903-5907.
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(2000)
Tetrahedron Lett
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Tezuka, Y.1
Ali, M.S.2
Banskota, A.H.3
Kadota, S.4
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2
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0035002563
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(b) Ali, M. S.; Tezuka, Y.; Banskota, A. H.; Kadota, S. J. Nat. Prod. 2001, 64, 491-496.
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(2001)
J. Nat. Prod
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Ali, M.S.1
Tezuka, Y.2
Banskota, A.H.3
Kadota, S.4
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3
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0030607152
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A large number of bioactive diarylheptanoid natural products were isolated recently by Kadota and co-workers from the seeds of Alpinia blepharocalyx K. Schum, a member of the Zingiberaceae family: (a) Kadota, S, Prasain, J. K, Li, J. X, Basnet, P, Dong, H, Tani, T, Namba, T. Tetrahedron Lett. 1996, 37, 7283-7286
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A large number of bioactive diarylheptanoid natural products were isolated recently by Kadota and co-workers from the seeds of Alpinia blepharocalyx K. Schum, a member of the Zingiberaceae family: (a) Kadota, S.; Prasain, J. K.; Li, J. X.; Basnet, P.; Dong, H.; Tani, T.; Namba, T. Tetrahedron Lett. 1996, 37, 7283-7286.
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4
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0030915895
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(b) Prasain, J. K.; Tezuka, Y.; Li, J. X.; Tanaka, K.; Basnet, P.; Dong, H.; Namba, T.; Kadota, S. Tetrahedron 1997, 53, 7833-7842.
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(1997)
Tetrahedron
, vol.53
, pp. 7833-7842
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Prasain, J.K.1
Tezuka, Y.2
Li, J.X.3
Tanaka, K.4
Basnet, P.5
Dong, H.6
Namba, T.7
Kadota, S.8
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5
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0031950635
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(c) Prasain, J. K.; Li, J.-X.; Tezuka, Y.; Tanaka, K.; Basnet, P.; Dong, H.; Namba, T.; Kadota, S. J. Nat. Prod. 1998, 61, 212-216.
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(1998)
J. Nat. Prod
, vol.61
, pp. 212-216
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Prasain, J.K.1
Li, J.-X.2
Tezuka, Y.3
Tanaka, K.4
Basnet, P.5
Dong, H.6
Namba, T.7
Kadota, S.8
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6
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0033518055
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(d) Gewali, M. B.; Tezuka, Y.; Banskota, A. H.; Ali, M. S.; Saiki, I.; Dong, H.; Kadota, S. Org. Lett. 1999, 1, 1733-1736.
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(1999)
Org. Lett
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, pp. 1733-1736
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Gewali, M.B.1
Tezuka, Y.2
Banskota, A.H.3
Ali, M.S.4
Saiki, I.5
Dong, H.6
Kadota, S.7
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7
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0035096066
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(e) Tezuka, Y.; Gewali, M. B.; Ali, M. S.; Banskota, A. H.; Kadota, S. J. Nat. Prod. 2001, 64, 208-213.
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(2001)
J. Nat. Prod
, vol.64
, pp. 208-213
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Tezuka, Y.1
Gewali, M.B.2
Ali, M.S.3
Banskota, A.H.4
Kadota, S.5
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8
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0035091234
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(f) Ali, M. S.; Tezuka, Y.; Awale, S.; Banskota, A. H.; Kadota, S. J. Nat. Prod. 2001, 64, 289-293.
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(2001)
J. Nat. Prod
, vol.64
, pp. 289-293
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Ali, M.S.1
Tezuka, Y.2
Awale, S.3
Banskota, A.H.4
Kadota, S.5
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9
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33645760404
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More recently, synthetic investigations by Rychnovsky and co-workers led to revised structures of some of the diarylheptanoids, calyxins L, F, M, and G: Tian, X.; Jaber, J. J.; Rychnovsky, S. D. J. Org. Chem. 2006, 71, 3176-3183.
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More recently, synthetic investigations by Rychnovsky and co-workers led to revised structures of some of the diarylheptanoids, calyxins L, F, M, and G: Tian, X.; Jaber, J. J.; Rychnovsky, S. D. J. Org. Chem. 2006, 71, 3176-3183.
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10
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33846435404
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2,8-dioxabicyclo
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As far as we know, blepharocalyxin D () is the only natural product known to possess a [4.4.0]decane core
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As far as we know, blepharocalyxin D (1) is the only natural product known to possess a 2,8-dioxabicyclo[4.4.0]decane core.
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, vol.1
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11
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0041346083
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There is one reference claiming to be a model study for synthesis of blepharocalyxin D (1): Li, W.; Mead, K. T.; Smith, L. T. Tetrahedron Lett. 2003, 44, 6351-6353.
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There is one reference claiming to be a model study for synthesis of blepharocalyxin D (1): Li, W.; Mead, K. T.; Smith, L. T. Tetrahedron Lett. 2003, 44, 6351-6353.
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12
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0141743328
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(a) Barry, C. S. J.; Crosby, S. R.; Harding, J. R.; Hughes, R. A.; King, C. D.; Parker, G. D.; Willis, C. L. Org. Lett. 2003, 5, 2429-2432.
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(2003)
Org. Lett
, vol.5
, pp. 2429-2432
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Barry, C.S.J.1
Crosby, S.R.2
Harding, J.R.3
Hughes, R.A.4
King, C.D.5
Parker, G.D.6
Willis, C.L.7
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13
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0001134456
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(b) Crosby, S. R.; Harding, J. R.; King, C. D.; Parker, G. D.; Willis, C. L. Org. Lett. 2002, 4, 577-580.
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(2002)
Org. Lett
, vol.4
, pp. 577-580
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Crosby, S.R.1
Harding, J.R.2
King, C.D.3
Parker, G.D.4
Willis, C.L.5
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14
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0141757166
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Hanawa, H.; Uraguchi, D.; Konishi, S.; Hashimoto, T.; Maruoka, K. Chem. Eur. J. 2003, 9, 4405-4413.
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(2003)
Chem. Eur. J
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Hanawa, H.1
Uraguchi, D.2
Konishi, S.3
Hashimoto, T.4
Maruoka, K.5
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15
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0001456053
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For extensive use of (O)-acetylmandelate NMR correlation, see: Lee, E.; Lee, Y. R.; Moon, B.; Kwon, O.; Shim, M. S.; Yun, J. S. J. Org. Chem. 1994, 59, 1444-1456.
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For extensive use of (O)-acetylmandelate NMR correlation, see: Lee, E.; Lee, Y. R.; Moon, B.; Kwon, O.; Shim, M. S.; Yun, J. S. J. Org. Chem. 1994, 59, 1444-1456.
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Garber, S. B.; Kingsbury, J. S.; Gray, B. L.; Hoveyda, A. H. J. Am. Chem. Soc. 2000, 122, 8168-8179.
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J. Am. Chem. Soc
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Garber, S.B.1
Kingsbury, J.S.2
Gray, B.L.3
Hoveyda, A.H.4
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22144498082
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For a recent discussion on oxonia-Cope rearrangement, see
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For a recent discussion on oxonia-Cope rearrangement, see: Jasti, R.; Anderson, C. D.; Rychnovsky, S. D. J. Am. Chem. Soc. 2005, 127, 9939-9945.
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(2005)
J. Am. Chem. Soc
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Jasti, R.1
Anderson, C.D.2
Rychnovsky, S.D.3
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Li, D.; Shi, F.; Peng, J.; Guo, S.; Deng, Y. J. Org. Chem. 2004, 69, 3582-3585.
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(2004)
J. Org. Chem
, vol.69
, pp. 3582-3585
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Li, D.1
Shi, F.2
Peng, J.3
Guo, S.4
Deng, Y.5
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0141678121
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For more discussions on Prins-pinacol reactions, see
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For more discussions on Prins-pinacol reactions, see: Overman, L. E.; Pennington, L. D. J. Org. Chem. 2003, 68, 7143-7157.
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J. Org. Chem
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Overman, L.E.1
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Baudin, J. B.; Hareau, G.; Julia, S. A.; Ruel, O. Tetrahedron Lett. 1991, 32, 1175-1178.
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(1991)
Tetrahedron Lett
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Baudin, J.B.1
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Ruel, O.4
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0037069714
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For a recent example of the use of lithium alkanethiolate in hot HMPA for aromatic ether demethylation, see: Nakatani, M, Nakamura, M, Suzuki, A, Inoue, M, Katoh, T. Org. Lett. 2002, 4, 4483-4486
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For a recent example of the use of lithium alkanethiolate in hot HMPA for aromatic ether demethylation, see: Nakatani, M.; Nakamura, M.; Suzuki, A.; Inoue, M.; Katoh, T. Org. Lett. 2002, 4, 4483-4486.
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