-
1
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0042227324
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-
note
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This version of lipid II is common to most Gram-positive bacteria. In Gram-negative bacteria, the lysine residue is replaced by mesodiaminopimelic acid (see ref 2).
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2
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0003607510
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Elsevier Biomedical: Amsterdam
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For a comprehensive review of bacterial cell wall biosynthesis, see: Ghuysen, J.-M.; Hackenbeck, R. Bacterial Cell Wall; Elsevier Biomedical: Amsterdam, 1994.
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(1994)
Bacterial Cell Wall
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Ghuysen, J.-M.1
Hackenbeck, R.2
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4
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5244279498
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-
The C(4) hydroxyl group is reported to be the least nucleophilic hydroxyl group in glucopyranose-based acceptors. See, for example: Toshima, K.; Tatsuta, K. Chem. Rev. 1993, 93, 1503.
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(1993)
Chem. Rev.
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Toshima, K.1
Tatsuta, K.2
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7
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4243588611
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(c) Kiso, M.; Kaneda, Y.; Shimizu, R.; Hasegawa, A. Carbohydr. Res. 1980, 83, C8.
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Carbohydr. Res.
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Kiso, M.1
Kaneda, Y.2
Shimizu, R.3
Hasegawa, A.4
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8
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0020485047
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(d) Kiso, M.; Kaneda, Y.; Shimizu, R.; Hasegawa, A. Carbohydr. Res. 1982, 104, 253.
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Carbohydr. Res.
, vol.104
, pp. 253
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Kiso, M.1
Kaneda, Y.2
Shimizu, R.3
Hasegawa, A.4
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9
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0022549328
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(e) Kusumoto, S.; Yamamoto, K.; Imoto, M.; Inage, M.; Tsujimoto, M.; Kotani, S.; Shiba, T. Bull. Chem. Soc. Jpn. 1986, 59, 1411.
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Bull. Chem. Soc. Jpn.
, vol.59
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Kusumoto, S.1
Yamamoto, K.2
Imoto, M.3
Inage, M.4
Tsujimoto, M.5
Kotani, S.6
Shiba, T.7
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10
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0000709659
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(f) Kusimoto, S.; Imoto, M.; Ogiku, T.; Shiba, T. Bull. Chem. Soc. Jpn. 1986, 59, 1419.
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Bull. Chem. Soc. Jpn.
, vol.59
, pp. 1419
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Kusimoto, S.1
Imoto, M.2
Ogiku, T.3
Shiba, T.4
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11
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0006169387
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(g) Farkas, J.; Ledvina, M.; Brokes, J.; Jezek, J.; Zajicek, J.; Zaoral, M. Carbohydr. Res. 1987, 163, 63.
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Farkas, J.1
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Jezek, J.4
Zajicek, J.5
Zaoral, M.6
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13
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0023339811
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(i) Kantoci, D.; Keglevic, D.; Derome, A. Carbohydr. Res. 1987, 162, 227.
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Kantoci, D.1
Keglevic, D.2
Derome, A.3
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15
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0000241814
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(k) Ledvina, M.; Farkas, J.; Zajicek, J.; Jezek, J.; Zaoral, M. Collect. Czech. Chem. Commun. 1989, 54, 2784.
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Ledvina, M.1
Farkas, J.2
Zajicek, J.3
Jezek, J.4
Zaoral, M.5
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17
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0032481622
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Hitchcock, S. A.; Eid, C. N.; Aikins, J. A.; Zia-Ebrahimi, M.; Blaszczak, L. C. J. Am. Chem. Soc. 1998, 120, 1916.
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Hitchcock, S.A.1
Eid, C.N.2
Aikins, J.A.3
Zia-Ebrahimi, M.4
Blaszczak, L.C.5
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18
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0033518559
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Zhang, Z.; Ollmann, I.; Ye, X.-S. Wischnat, R.; Baasov, T.; Wong, C.-H. J. Am. Chem. Soc. 1999, 121, 734.
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Zhang, Z.1
Ollmann, I.2
Ye, X.-S.3
Wischnat, R.4
Baasov, T.5
Wong, C.-H.6
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20
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0001413921
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For a preparation of 5, see: Jeanloz, R. W.; Walker, E.; Sinaÿ, P. Carbohydr. Res. 1968, 6, 184.
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(1968)
Carbohydr. Res.
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, pp. 184
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Jeanloz, R.W.1
Walker, E.2
Sinaÿ, P.3
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21
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0028840018
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DeNinno, M. P.; Etienne, J. B.; Duplantier, K. C. Tetrahedron Lett. 1995, 36, 669.
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(1995)
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, vol.36
, pp. 669
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DeNinno, M.P.1
Etienne, J.B.2
Duplantier, K.C.3
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22
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0001377184
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Donor 3 may be prepared in three steps from commercially available glucosamine. See: Imoto, M.; Yoshimura, H.; Shimoto, T.; Sakaguchi, N.; Kusumoto, S.; Shiba, T. Bull. Chem. Soc. Jpn. 1987, 60, 2205.
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(1987)
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, vol.60
, pp. 2205
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Imoto, M.1
Yoshimura, H.2
Shimoto, T.3
Sakaguchi, N.4
Kusumoto, S.5
Shiba, T.6
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23
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0030750991
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Yang, G.; Ding, X.; Kong, F. Tetrahedron Lett. 1997, 38, 6725.
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(1997)
Tetrahedron Lett.
, vol.38
, pp. 6725
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Yang, G.1
Ding, X.2
Kong, F.3
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24
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0041727006
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-
note
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13C NMR, and IR) was consistent with the assigned structures.
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