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1
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0013553348
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(Moos, W.H.; Pavia, M.R.; Kay,B.K.; Ellington, A.D., editors), Escom Sciences Publishers, Leiden
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1. For a recent review see: Hall, S.E. in Annual Report in Combinatorial Chemistry and Molecular Diversity, Vol. 1, (Moos, W.H.; Pavia, M.R.; Kay,B.K.; Ellington, A.D., editors), Escom Sciences Publishers, Leiden, 1997, 30-40.
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(1997)
Annual Report in Combinatorial Chemistry and Molecular Diversity Vol. 1
, vol.1
, pp. 30-40
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Hall, S.E.1
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3
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0030998777
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3. Siegel, M.G.; Hahn, P.J.; Dressman, B.A.; Fritz, J.E.; Grunwell, J.R.; Kaldor, S.W. Tetrahedron Lett. 1997 38, 3357.
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(1997)
Tetrahedron Lett.
, vol.38
, pp. 3357
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Siegel, M.G.1
Hahn, P.J.2
Dressman, B.A.3
Fritz, J.E.4
Grunwell, J.R.5
Kaldor, S.W.6
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4
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0030607141
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4. Kaldor, S.W.; Siegel, M.G.; Fritz, J.E.; Dressman, B.A.; Hahn, P.J. Tetrahedron Lett. 1996, 37, 7193.
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(1996)
Tetrahedron Lett.
, vol.37
, pp. 7193
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Kaldor, S.W.1
Siegel, M.G.2
Fritz, J.E.3
Dressman, B.A.4
Hahn, P.J.5
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7
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0013547498
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US 4,638,032
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7. Benner, S.A. 1987, US 4,638,032.
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(1987)
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Benner, S.A.1
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8
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0013517599
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A low cross-linked polystyrene bead (1-2% divinyl benzene) can be seen as a sponge with the majority (>95%) of the reactive sites located within the cavities of the bead. Solvents such as methylene chloride cause the cavities within the bead to greatly expand, allowing reagents and starting materials to freely enter and leave the bead through the process of diffusion
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8. A low cross-linked polystyrene bead (1-2% divinyl benzene) can be seen as a sponge with the majority (>95%) of the reactive sites located within the cavities of the bead. Solvents such as methylene chloride cause the cavities within the bead to greatly expand, allowing reagents and starting materials to freely enter and leave the bead through the process of diffusion.
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9
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0013482351
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US 5,834,121
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9. Sucholeiki, I.; Margetts, G.; Roberts, M. 1998, US 5,834,121.
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(1998)
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Sucholeiki, I.1
Margetts, G.2
Roberts, M.3
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10
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0013552371
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US 5,684,130
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10. Sucholeiki, I., 1997, US 5,684,130.
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(1997)
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Sucholeiki, I.1
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11
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0013485476
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The level of substitution was determined by iodine elemental analysis
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11. The level of substitution was determined by iodine elemental analysis.
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12
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0013555314
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The reaction was followed by taking aliquots at timed intervals and separating the components using reversed-phase HPLC (C-18 radial compression column) and 254 nm detection
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12. The reaction was followed by taking aliquots at timed intervals and separating the components using reversed-phase HPLC (C-18 radial compression column) and 254 nm detection.
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13
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0027272147
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The loading capacity was determined to be 0.6 mmoles amine/gram by spectrophotometric assay of the released fluorenylmethoxycarbonyl (Fmoc) group according to
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13. The loading capacity was determined to be 0.6 mmoles amine/gram by spectrophotometric assay of the released fluorenylmethoxycarbonyl (Fmoc) group according to Green, J.; Bradley, K. Tetrahedron 1993, 49, 4141.
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(1993)
Tetrahedron
, vol.49
, pp. 4141
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Green, J.1
Bradley, K.2
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14
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0013545206
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note
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4·1.35 TFA: C, 41.50; H, 5.91; N, 14.48; F, 15.91. Found: C, 41.17; H, 5.80; N, 12.98; F, 15.87.
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