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0001212549
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Willson T.M., Kocienski P., Jarowicki K., Isaac K., Faller A., Campbell S.F., and Bordner J. Tetrahedron 46 (1990) 1757-1766
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Willson, T.M.1
Kocienski, P.2
Jarowicki, K.3
Isaac, K.4
Faller, A.5
Campbell, S.F.6
Bordner, J.7
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5
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53349095610
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Delforge D., Dieu M., Delaive E., Art M., Gillon B., Devreese B., Raes M., Van Beeumen J., and Remacle J. Lett. Pept. Sci. 3 (1996) 89-97
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Delforge, D.1
Dieu, M.2
Delaive, E.3
Art, M.4
Gillon, B.5
Devreese, B.6
Raes, M.7
Van Beeumen, J.8
Remacle, J.9
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6
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63449121566
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Nuijens T., Cusan C., Kruijtzer J.A.W., Rijkers D.T.S., Liskamp R.M.J., and Quaedflieg P.J.L.M. Synthesis 5 (2009) 809-814
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(2009)
Synthesis
, vol.5
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Nuijens, T.1
Cusan, C.2
Kruijtzer, J.A.W.3
Rijkers, D.T.S.4
Liskamp, R.M.J.5
Quaedflieg, P.J.L.M.6
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17
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0024841786
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Xaus N., Clapés P., Bardaji E., Torres X., Horba X., Mata J., and Valencia G. Tetrahedron 45 (1989) 7421-7426
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(1989)
Tetrahedron
, vol.45
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-
Xaus, N.1
Clapés, P.2
Bardaji, E.3
Torres, X.4
Horba, X.5
Mata, J.6
Valencia, G.7
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18
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3543118867
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Obtained from Novozymes, 10 wt % Alcalase solution, 6.75 €/kg
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Obtained from Novozymes, 10 wt % Alcalase solution, 6.75 €/kg. Maurer K.H. Curr. Opin. Biotechnol. 15 (2004) 330
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(2004)
Curr. Opin. Biotechnol.
, vol.15
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Maurer, K.H.1
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19
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0014409072
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Smith E.L., DeLange R.J., Evans W.H., Landon M., and Markland F.S. J. Biol. Chem. 243 (1968) 2184
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Smith, E.L.1
DeLange, R.J.2
Evans, W.H.3
Landon, M.4
Markland, F.S.5
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23
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64749089526
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note
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2O and 85% of 0.1 mL/L formic acid in acetonitrile as eluent).
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-
-
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24
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64749083055
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note
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3 (2×). Additional column chromatography with EtOAc/n-hexane mixtures was performed if necessary. The purity of the β- or γ-ester of the N-protected Asp or Glu derivatives, respectively, was >98% as determined by HPLC.
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27
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64749107194
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note
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3) δ = -1.5, 17.3, 36.7, 50.4, 53.5, 64.5, 136.2, 159.9, 170.9, 175.4.
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-
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29
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0034742736
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Boc-Asp(OAll)-OH, Fmoc-Asp(OAll)-OH and Fmoc-Glu(OAll)-OH:
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Boc-Asp(OAll)-OH, Fmoc-Asp(OAll)-OH and Fmoc-Glu(OAll)-OH:. Webster K.L., Maude A.B., O'Donnell M.E., Mehrotra A.P., and Gani D. J. Chem. Soc., Perkin Trans. 1 (2001) 1673-1695
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(2001)
J. Chem. Soc., Perkin Trans. 1
, pp. 1673-1695
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Webster, K.L.1
Maude, A.B.2
O'Donnell, M.E.3
Mehrotra, A.P.4
Gani, D.5
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30
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64749095957
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note
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Boc-Glu(OAll)-OH: CAS 132286-79-4.
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31
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64749105095
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WO Pat. Appl. No, 082890, CAS No. 147:210280 HCA
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Eggen, I.F.; Boeriu, C.G. WO Pat. Appl. No. 2007 082890, CAS No. 147:210280 HCA.
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(2007)
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Eggen, I.F.1
Boeriu, C.G.2
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32
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64749101881
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note
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3 (2×). The NMR data were identical to those of the commercially obtained compound.
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33
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0028000937
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4) and concentrated in vacuo. NMR data corresponded to those reported by:
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4) and concentrated in vacuo. NMR data corresponded to those reported by:. Sears P., Schuster M., Wang P., Witte K., and Wong C.H. J. Am. Chem. Soc. 116 (1994) 6521-6530
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(1994)
J. Am. Chem. Soc.
, vol.116
, pp. 6521-6530
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Sears, P.1
Schuster, M.2
Wang, P.3
Witte, K.4
Wong, C.H.5
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34
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0034614461
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4) and concentrated in vacuo. NMR data corresponded to those reported by
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4) and concentrated in vacuo. NMR data corresponded to those reported by. David C., Bischoff L., Roques B.P., and Fournie-Zaluski M.C. Tetrahedron 56 (1999) 209-215
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(1999)
Tetrahedron
, vol.56
, pp. 209-215
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David, C.1
Bischoff, L.2
Roques, B.P.3
Fournie-Zaluski, M.C.4
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35
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64749098290
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note
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tBu)-OH: CAS. 5545-52-8.
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