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3. Alvarez, M. E.; Huock, D. R.; White, C. B.; Brownell, J. E.; Bobko, M. A.; Rodger, C. A.; Stawicki, M. B.; Sun, H. H.; Gillum, A. M.; Cooper, R. J. Antibiot. 1994, 47, 1195.
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4
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Solid-phase mix-and-split synthesis on Wang resin, post-cleavage cyclization in toluene, 110 °C
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4. Gordon, D. W.; Steele, J. Bioorg. Med. Chem. Lett. 1995, 5, 47. (Solid-phase mix-and-split synthesis on Wang resin, post-cleavage cyclization in toluene, 110 °C.)
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0010410840
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U.S. Patent 5 324 483, 1994. Parallel solid-phase synthesis of 40 proline-containing piperazinediones, using Merrifield resin
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8. Cody, D. R.; DeWitt, S. H. H.; Hodges, J. C.; Kiely, J. S.; Moos, W. H.; Pavia, M. R.; Roth, B. D.; Schroeder, M. C.; Stankovic, C. J. U.S. Patent 5 324 483, 1994. (Parallel solid-phase synthesis of 40 proline-containing piperazinediones, using Merrifield resin.)
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Cody, D.R.1
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Stankovic, C.J.9
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9
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0030252432
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Solid-phase mix-and-split synthesis on Wang resin, simultaneous cyclization/cleavage, 2 M AcOH in 2-BuOH, 110 °C
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9. Goodfellow, V. S.; Laudeman, C. P.; Gerrity, J. I.; Burkard, M.; Strobel, E.; Zuzack, J. S.; McLeod, D. A. Mol. Diversity 1996, 2, 97. (Solid-phase mix-and-split synthesis on Wang resin, simultaneous cyclization/cleavage, 2 M AcOH in 2-BuOH, 110 °C.)
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Goodfellow, V.S.1
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Strobel, E.5
Zuzack, J.S.6
McLeod, D.A.7
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10
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0031000559
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Solid-phase synthesis on Tentagel-S OH or PAM resin, simultaneous cyclization/cleavage, 1/1 toluene/EtOH with 1% AcOH or 4% Et3N, 20 °C
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10. Szardenings, A. K.; Burkoth, T. S.; Lu, H. H.; Tien, D. W.; Campbell, D. A. Tetrahedron 1997, 19, 6573. (Solid-phase synthesis on Tentagel-S OH or PAM resin, simultaneous cyclization/cleavage, 1/1 toluene/EtOH with 1% AcOH or 4% Et3N, 20 °C.)
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Szardenings, A.K.1
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Campbell, D.A.5
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12
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0010409115
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note
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12. Advanced ChemTech, 5609 Fern Valley Road, Louisville, KY 40228, U.S.A.
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13
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0010330307
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note
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2), p-nitro-phenylalanine; 2-Abz, 2-aminobenzoic acid.
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14
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0030202425
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note
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14. HPLC/UV/ELSD analyses employed Perkin-Elmer Pecosphere 3X3C C-18 reverse-phase cartridge columns (0.46 × 3.3 cm), at 3.0 mL/min, with an elution gradient of 0-70% aqueous acetonitrile (containing 0.1% TFA) over 7 min, then 70-100% over 0.5 min, then 100% for 2.5 min, with a 5-min equilibration period; UV detection was at 200 nm, and a Sedere Sedex Model 55 was used for evaporative light-scattering detection (ELSD). In general, the purity based on UV detection (200 nm) was somewhat less than that based on ELSD; however, ELSD is established to be a more "universal" detector, giving near-equivalent response to a variety of compounds (Kibbey, C. E. Mol. Diversity 1995, 1, 247). A Finnigan LCQ was used for LC/MS analyses.
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15
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0029128552
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17. Mayer, J. P.; Zhang, J.; Bjergard, K.; Lenz, D. M.; Gaudino, J. J. Tetrahedron Lett. 1996, 37, 8081.
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Mayer, J.P.1
Zhang, J.2
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Lenz, D.M.4
Gaudino, J.J.5
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18
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0010411250
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PCT Int. Appl. WO 9 422 840, 1994
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2Ph: Day, R. A.; Tharp, R. L.; Madis, M. E.; Wallace, J. A.; Silanee, A.; Hurt, P.; Mastruserio, N. Pept. Res. 1990, 3, 169.
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Hodge, C.A.1
Fernandez, C.H.2
Jadhav, P.K.3
Lam, P.Y.-S.4
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19
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0025449810
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2Ph: Day, R. A.; Tharp, R. L.; Madis, M. E.; Wallace, J. A.; Silanee, A.; Hurt, P.; Mastruserio, N. Pept. Res. 1990, 3, 169.
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Day, R.A.1
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Silanee, A.5
Hurt, P.6
Mastruserio, N.7
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