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84891309023
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See for recent examples: D. Seebach, J. L. Matthews, Chem. Commun. 1997, 2015; D. H. Appella, L. A. Christianson, D. A. Klein, D. Powell, X. Huang, J. J. Barchi Jr., S. H. Gellman, Nature 1997, 387, 381; C. Gennari, B. Salom, D. Potenza, C. Longari, E. Fioravanzo, O. Carugo, N. Sardone, Chem. Eur. J. 1996, 2, 644; J. S. Novick, M. Pairish, I. Q. Lee, D L. Holmes, J. W. Ziller, J. Am. Chem. Soc. 1997, 119, 5413.
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0030811193
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See for recent examples: D. Seebach, J. L. Matthews, Chem. Commun. 1997, 2015; D. H. Appella, L. A. Christianson, D. A. Klein, D. Powell, X. Huang, J. J. Barchi Jr., S. H. Gellman, Nature 1997, 387, 381; C. Gennari, B. Salom, D. Potenza, C. Longari, E. Fioravanzo, O. Carugo, N. Sardone, Chem. Eur. J. 1996, 2, 644; J. S. Novick, M. Pairish, I. Q. Lee, D L. Holmes, J. W. Ziller, J. Am. Chem. Soc. 1997, 119, 5413.
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M. Falorni, G. Giacomelli, G. Synlett, 1996, 143-144; F. D'Aniello, M. Falorni, A. Mann, M. Taddei, Tetrahedron: Asymmetry 1996, 7, 1217-1226; M. Falorni, A. Porcheddu, G. Giacomelli, Tetrahedron: Asymmetry 1996, 7, 1999-2005; M. Falorni, A. Porcheddu, G. Giacomelli, Tetrahedron: Asymmetry 1997, 8, 1633-1639.
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M. Falorni, G. Giacomelli, G. Synlett, 1996, 143-144; F. D'Aniello, M. Falorni, A. Mann, M. Taddei, Tetrahedron: Asymmetry 1996, 7, 1217-1226; M. Falorni, A. Porcheddu, G. Giacomelli, Tetrahedron: Asymmetry 1996, 7, 1999-2005; M. Falorni, A. Porcheddu, G. Giacomelli, Tetrahedron: Asymmetry 1997, 8, 1633-1639.
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M. Falorni, G. Giacomelli, G. Synlett, 1996, 143-144; F. D'Aniello, M. Falorni, A. Mann, M. Taddei, Tetrahedron: Asymmetry 1996, 7, 1217-1226; M. Falorni, A. Porcheddu, G. Giacomelli, Tetrahedron: Asymmetry 1996, 7, 1999-2005; M. Falorni, A. Porcheddu, G. Giacomelli, Tetrahedron: Asymmetry 1997, 8, 1633-1639.
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M. Falorni, G. Giacomelli, G. Synlett, 1996, 143-144; F. D'Aniello, M. Falorni, A. Mann, M. Taddei, Tetrahedron: Asymmetry 1996, 7, 1217-1226; M. Falorni, A. Porcheddu, G. Giacomelli, Tetrahedron: Asymmetry 1996, 7, 1999-2005; M. Falorni, A. Porcheddu, G. Giacomelli, Tetrahedron: Asymmetry 1997, 8, 1633-1639.
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0030062528
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17
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85080549132
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note
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1H NMR spectroscopy.
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18
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0003803058
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Springer-Verlag, Berlin
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This compound was prepared directly from histidine modifying the procedure reported for L-histidine methyl ester: M. Bodanszky, A. Bodanszky, in The Practice of Peptide Synthesis 2nd ed., Springer-Verlag, Berlin, 1994, p. 60.
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(1994)
The Practice of Peptide Synthesis 2nd Ed.
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Bodanszky, M.1
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0032491014
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A new class of oxazole-based scaffolds was recently reported: D. Mink, S. Mecozzi, J. Rebek, Jr., Tetrahedron Lett. 1998, 39, 5709-5712.
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M. Falorni, G. Giacomelli, F. Nieddu, M. Taddei, M. Tetrahedron Lett. 1997, 38, 4663-4666; M. Falorni, G. Giacomelli, L. Mameli, A. Porcheddu, Tetrahedron Lett. 1998, 39, 7607-7610.
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Falorni, M.1
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0032497706
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M. Falorni, G. Giacomelli, F. Nieddu, M. Taddei, M. Tetrahedron Lett. 1997, 38, 4663-4666; M. Falorni, G. Giacomelli, L. Mameli, A. Porcheddu, Tetrahedron Lett. 1998, 39, 7607-7610.
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Falorni, M.1
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22
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85080559580
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note
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6 (358.21): calcd. C 56.97, H 8.44, N 7.82; found C 56.92, H 8.39, N 7.86.
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-
-
-
23
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85080596075
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note
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3, 50 °C): δ = 6.73 (br. s, 1 H, NH), 7.14 (s, 1 H), 7.22 (br. s, 1 H, NH), 7.56 (br. s, 1 H, NH), 7.66 (s, 1 H), 8.26 (br. s, 1 H, NH).
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