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24
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26
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0042198757
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Bonache M.A., Gerona-Navarro G., García-Aparicio C., Alías M., Martín-Martínez M., García-López M.T., López P., Cativiela C., and González-Muñiz R. Tetrahedron: Asymmetry 14 (2003) 2161-2169
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García-López, M.T.6
López, P.7
Cativiela, C.8
González-Muñiz, R.9
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27
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0037561625
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Bonache M.A., Gerona-Navarro G., Martín-Martínez M., García-López M.T., López P., Cativiela C., and González-Muñiz R. Synlett (2003) 1007-1011
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López, P.5
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28
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28544448047
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Bonache M.A., López P., Martín-Martínez M., García-López M.T., Cativiela C., and González-Muñiz R. Tetrahedron 62 (2006) 130-138
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García-López, M.T.4
Cativiela, C.5
González-Muñiz, R.6
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29
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33745730514
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note
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Compounds 1, 2, 8, 9, and 15 were previously described by us (see Refs. 23 and 24).
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31
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0037450499
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Lam P.Y.S., Bonne D., Vincent G., Clark C.G., and Combs A.P. Tetrahedron Lett. 44 (2003) 1691-1694
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Lam, P.Y.S.1
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Vincent, G.3
Clark, C.G.4
Combs, A.P.5
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32
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0032501446
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Attempts to use (p-methoxy)phenyl bromide as the N-arylating agent under palladium catalysis resulted in better yield of compound 7, but it was obtained in totally racemic form. For references related to this palladium catalyzed N-arylation procedures, see:
-
Attempts to use (p-methoxy)phenyl bromide as the N-arylating agent under palladium catalysis resulted in better yield of compound 7, but it was obtained in totally racemic form. For references related to this palladium catalyzed N-arylation procedures, see:. Ma D., Zhang Y., Yao J., Wu S., and Tao F. J. Am. Chem. Soc. 120 (1998) 12459-12467
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Ma, D.1
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Yao, J.3
Wu, S.4
Tao, F.5
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33
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0034847422
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Clement J.B., Hayes J.F., Sheldrake H.M., Sheldrake P.W., and Wells A.S. Synlett (2001) 1423-1427
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(2001)
Synlett
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Clement, J.B.1
Hayes, J.F.2
Sheldrake, H.M.3
Sheldrake, P.W.4
Wells, A.S.5
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34
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33745730513
-
-
note
-
BTPP: tert-Butylimino-tri(pyrrolidino)phosphorane. BEMP: 2-tert-Butylimino-2-diethylamino-1,3-dimethylperhydro-1,3,2-diaza-phosphorine.
-
-
-
-
35
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33745730508
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-
note
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4: C, 70.14; H, 5.89; N, 4.31. Found: C, 70.15, H, 5.75, N, 4.65.
-
-
-
-
36
-
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33745688273
-
-
note
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4: C, 71.37; H, 6.56; N, 3.96. Found: C, 71.45, H, 6.75, N, 3.65.
-
-
-
-
37
-
-
33745702464
-
-
note
-
4: C, 70.14; H, 5.89; N, 4.31. Found: C, 70.45, H, 5.65, N, 4.25.
-
-
-
-
38
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0037204722
-
-
The assignment of Phe-derived β-lactams was unambiguously done by conversion into α-benzyl aspartic acids of known configuration:
-
The assignment of Phe-derived β-lactams was unambiguously done by conversion into α-benzyl aspartic acids of known configuration:. Gerona-Navarro G., García-López M.T., and González-Muñiz R. J. Org. Chem. 67 (2002) 3953-3956
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(2002)
J. Org. Chem.
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Gerona-Navarro, G.1
García-López, M.T.2
González-Muñiz, R.3
-
40
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0025801244
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González-Muñiz R., Cornille F., Bergeron F., Ficheux D., Pothier J., Durieux C., and Roques B.P. Int. J. Pept. Protein Res. 37 (1991) 331-340
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(1991)
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González-Muñiz, R.1
Cornille, F.2
Bergeron, F.3
Ficheux, D.4
Pothier, J.5
Durieux, C.6
Roques, B.P.7
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