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14
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0343099229
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++1). 23
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-).
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15
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0343971062
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2O (0.3 mL) was heated at 60 °C for 4 h. The solvent was removed and coevaporated with toluene. The residue was purified on silica gel
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max 260.0 nm. HRMS (FAB) calcd 319.1519, found 319.1510.
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16
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0342664922
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2O (0.1 mL)
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max 271.0 nm. HRMS (FAB) calcd 353.1129, found 353.1139.
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17
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0342664920
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3 to furnish 0.13 g of product 28. To a solution of 28 (0.025 g, 0.08 mmol) in MeOH (2 mL), was added cyclopentylamine (0.04 mL, 0.4 mmol) and the mixture was stirred at rt for 8 h. Solvent was removed under vacuum and the residue was purified
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3OD) δ 8.46 (s, 1H, C-8), 7.77 (s, 1H), 7.59 (d, 1H, J=7.81 Hz), 7.39 (d, 1H, J=7.81 Hz), 7.09 (t, 1H, J=7.81 Hz), 4.96 (d, 1H, J=5.86 Hz), 4.7 (s, 2H), 4.27 (d, 1H, J=11.72 Hz), 3.36 (d, 1H, J=11.72 Hz), 2.1-1.96 (m, 1H), 1.9-1.7 (m, 1H), 1.7-1.6 (m, 1H), 1.04-1.01 (m, 1H), 0.82-0.74 (m, 1H). HRMS (FAB) calcd 512.0350, found 512.0358.
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19
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0032493423
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Mogensen J.P., Roberts S.M., Bowler A.N., Thomsen C., Knutsen L.J. Bioorg. Med. Chem. Lett. 8:1998;1767.
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Mogensen, J.P.1
Roberts, S.M.2
Bowler, A.N.3
Thomsen, C.4
Knutsen, L.J.5
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20
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0033403349
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Marquez V.E., Russ P., Alonso R., Siddiqui M.A., Hernandez S., George C., Nicklaus M.C., Dai F., Ford H. Helv. Chim. Acta. 82:1999;2119.
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Marquez, V.E.1
Russ, P.2
Alonso, R.3
Siddiqui, M.A.4
Hernandez, S.5
George, C.6
Nicklaus, M.C.7
Dai, F.8
Ford, H.9
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