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L.A. Carpino, M. Ismail, G.A. Truran, E.M.E. Mansour, S. Iguchi, D. Ionescu, A. El-Faham, C. Riemer, and R. Warrass J. Org. Chem. 64 1999 4324
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6
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4444357327
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note
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If deblocking is difficult the instrument is programmed to add additional deblocking and coupling steps
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10
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0036462499
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L.A. Carpino, H. Imazumi, A. El-Faham, F.J. Ferrer, C. Zhang, Y. Lee, B.M. Foxman, P. Henklein, C. Hanay, C. Mugge, H. Wenschuh, J. Klose, M. Beyermann, and M. Bienert Angew. Chem., Int. Ed. 41 2002 441 footnote 24
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Henklein, P.8
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Mugge, C.10
Wenschuh, H.11
Klose, J.12
Beyermann, M.13
Bienert, M.14
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11
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0017876296
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See for example: M. Fujino, M. Wakimasu, S. Shinagawa, C. Kitada, and H. Yajima Chem. Pharm. Bull. 26 1978 539
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12
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37049090173
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For the use of acid fluorides for the acylation of polymer supported hydroxyl functions see: D. Granitza, M. Beyermann, H. Wenschuh, H. Haber, L.A. Carpino, G.A. Truran, and M. Bienert J. Chem. Soc. Chem. Commun. 1995 2223
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Bienert, M.7
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13
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0028847274
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For related work on the use of the O→N rearrangement in the development of water-soluble prodrugs see: R. Oliyai, and V.J. Stella Bioorg. Med. Chem. Lett. 5 1995 2735
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Stella, V.J.2
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0036973331
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Y. Hamada, J. Ohtake, Y. Sohma, T. Kimura, Y. Hayashi, and Y. Kiso Bioorg. Med. Chem. 10 2002 4155 While this paper was being prepared for publication Kiso and co-workers (
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Hamada, Y.1
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15
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1642458245
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Y. Sohma, M. Sasaki, Y. Hayashi, T. Kimura, and Y. Kiso Chem. Commun. 22 2004 124) published a similar recommendation for the synthesis of difficult peptides
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16
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0001502832
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the very first example of the use of related methodology for the synthesis of a difficult peptide was described by Horikawa and Ohfune and co-workers (M. Horikawa, T. Nakajima, and Y. Ohfune Synlett 1998 609
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Synlett
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Horikawa, M.1
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17144466895
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M. Horikawa, Y. Shigeri, N. Yumoto, S. Yoshikawa, T. Nakajima, and Y. Ohfune Bioorg Med. Chem. Lett. 8 1998 2027)
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M. Mutter, A. Nefzi, T. Sato, X. Sun, F. Wahl, and T. Wöhr Peptide Res. 8 1995 145
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