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0037424684
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Chen P., Norris D., Haslow K.D., Murali Dhar T.G., Pitts W.J., Watterston S.H., Cheney D.L., Bassolino D.A., Fleener C.A., Rouleau K.A., Hollenbaugh D.L., Townsend R.M., Barrish J.C., Iwanowicz E.J. Bioorg. Med. Chem. Lett. 13:2003;1345-1348.
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7
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0037213348
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For a recent compilation of methods, see:
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For a recent compilation of methods, see: Lee J.C., Choi H.J., Lee Y.C. Tetrahedron Lett. 44:2003;123-125.
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Lee, J.C.1
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8
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0001419996
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11
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85031133248
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note
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13C NMR (75 MHz) δ 157.6, 156.6, 103.0, 77.1, 65.8, 48.5, 36.2, 26.1, -0.4; FIMS m/z 312 (M+).
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-
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12
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85031132969
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note
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3N·HCl) enabled reactions to occur smoothly at rt and prevented side reactions involving the active methylene group of 1 .
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-
-
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13
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85031132081
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note
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3) δ 158.1, 157.0, 102.7, 68.0, 66.2, 60.1, 48.7, 46.8, 32.6, 25.9, 22.4; IR (film) 2930, 2850, 1610, 1555, 1455; FABMS m/z 320 (M-1).
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-
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14
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85031142328
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A representative cross-section of primary and secondary amines gave good results in an earlier study with substituted isocyanoacetamides (Ref. 6a)
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A representative cross-section of primary and secondary amines gave good results in an earlier study with substituted isocyanoacetamides (Ref. 6a).
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15
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0028229963
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Hayashi M., Yoshiga T., Nakatani K., Ono K., Oguni N. Tetrahedron. 50:1994;2821-2830.
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Tetrahedron
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Hayashi, M.1
Yoshiga, T.2
Nakatani, K.3
Ono, K.4
Oguni, N.5
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16
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85031138259
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Spectroscopic and physical characterization data for new compounds are included in Supplementary Data, which is available on the Web
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Spectroscopic and physical characterization data for new compounds are included in Supplementary Data, which is available on the Web.
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18
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0033118907
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Roy R.S., Gehring A.M., Milne J.C., Belshaw P.J., Walsh C.T. Nat. Prod. Rep. 16:1999;249-263.
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Roy, R.S.1
Gehring, A.M.2
Milne, J.C.3
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Walsh, C.T.5
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