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1
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85030275873
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The configuration of the 5-hydroxypipecolic acid derivatives is indicated in one of the following ways: position 5: cis-and irons-hydroxy or 5R and 5S, respectively; position 2 : D and L-aminoacid or 2R and 2S, respectively
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1. The configuration of the 5-hydroxypipecolic acid derivatives is indicated in one of the following ways: position 5: cis-and irons-hydroxy or 5R and 5S, respectively; position 2 : D and L-aminoacid or 2R and 2S, respectively.
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-
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4
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0001132035
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(c) Goas G., Larher F., Goas M., C. R. Acad. Sc. Paris 1970, 271, 1368.
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(1970)
C. R. Acad. Sc. Paris
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, pp. 1368
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Goas, G.1
Larher, F.2
Goas, M.3
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5
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0011883252
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Eds. L. Reinhold and Y. Liwischitz, Wiley London
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(d) Fowden L., Progress in Phytochemistry, Eds. L. Reinhold and Y. Liwischitz, Wiley London, 1970, 2, 203.
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(1970)
Progress in Phytochemistry
, vol.2
, pp. 203
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Fowden, L.1
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7
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0000711165
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(f) Despontin J., Marlier M., and Dardenne G., Phytochemistry 1977, 16, 387.
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(1977)
Phytochemistry
, vol.16
, pp. 387
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Despontin, J.1
Marlier, M.2
Dardenne, G.3
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8
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0018332289
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3. Mester L., Szabados L., Mester M., Yadav N., Planta Medica 1979, 35, 339.
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(1979)
Planta Medica
, vol.35
, pp. 339
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Mester, L.1
Szabados, L.2
Mester, M.3
Yadav, N.4
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9
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0026808484
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4. (a) Fujii T., Murai M., Morimoto H., Maeda Y., Yamaoka M., Hagiwara D., Miyake H., Ikari N., Matsuo M., Br. J. Pharmacol. 1992, 107, 785.
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(1992)
Br. J. Pharmacol.
, vol.107
, pp. 785
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-
Fujii, T.1
Murai, M.2
Morimoto, H.3
Maeda, Y.4
Yamaoka, M.5
Hagiwara, D.6
Miyake, H.7
Ikari, N.8
Matsuo, M.9
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10
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0027945211
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(b) Koehn F. E., McConnell O. J., Longley R. E., Sennett S. H., and Reed J. K., J. Med. Chem. 1994, 37, 3181.
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(1994)
J. Med. Chem.
, vol.37
, pp. 3181
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Koehn, F.E.1
McConnell, O.J.2
Longley, R.E.3
Sennett, S.H.4
Reed, J.K.5
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11
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0025296462
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5. (a) Copeland T. D., Wondrak E. M., Tozser J., Roberts M. M., Oroszlan S., Biochem. Biophys. Res. Commun. 1990, 169, 310.
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(1990)
Biochem. Biophys. Res. Commun.
, vol.169
, pp. 310
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Copeland, T.D.1
Wondrak, E.M.2
Tozser, J.3
Roberts, M.M.4
Oroszlan, S.5
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12
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0025673805
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-
(b) Itazaki H., Nagashima K., Sugita K., Yoshida H., Kawamura Y., Yasuda Y., Matsumoto K., Ishii K., Uotani N., Nakai H., Terui A., Yoshimatsu S., Ikenishi Y., Nakagawa Y., J. Antibiotics 1990, 1524.
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(1990)
J. Antibiotics
, pp. 1524
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Itazaki, H.1
Nagashima, K.2
Sugita, K.3
Yoshida, H.4
Kawamura, Y.5
Yasuda, Y.6
Matsumoto, K.7
Ishii, K.8
Uotani, N.9
Nakai, H.10
Terui, A.11
Yoshimatsu, S.12
Ikenishi, Y.13
Nakagawa, Y.14
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14
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0000540071
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(b) Fujita Y., Irreverre F., Witkop B., J. Am. Chem. Soc. 1964, 86, 1844.
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(1964)
J. Am. Chem. Soc.
, vol.86
, pp. 1844
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-
Fujita, Y.1
Irreverre, F.2
Witkop, B.3
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15
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0001322725
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(c) Callens R. E. A., Anteunis M. J. O., Reyniers F., Bull. Soc. Chim. Belg. 1982, 91, 713.
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(1982)
Bull. Soc. Chim. Belg.
, vol.91
, pp. 713
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Callens, R.E.A.1
Anteunis, M.J.O.2
Reyniers, F.3
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20
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0025818723
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7. Tabcheh M., El. Achqar A., Pappalardo L., Roumestant M. L., and Viallefont Ph., Tetrahedron 1991, 47, 4611.
-
(1991)
Tetrahedron
, vol.47
, pp. 4611
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-
Tabcheh, M.1
El Achqar, A.2
Pappalardo, L.3
Roumestant, M.L.4
Viallefont, Ph.5
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21
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85030278651
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3OH, which was possible only with pyrrolidine structure); 190; 170; 146
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3OH, which was possible only with pyrrolidine structure); 190; 170; 146.
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23
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85030268870
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2Ph), 7.26 (5H, s, Ph)
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2Ph), 7.26 (5H, s, Ph).
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24
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21844513090
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11. Cavelier F., Rolland M., Verducci J., Org. prep. proc. int. Briefs 1994, 26, 608.
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(1994)
Org. Prep. Proc. Int. Briefs
, vol.26
, pp. 608
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Cavelier, F.1
Rolland, M.2
Verducci, J.3
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25
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84981003593
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12. 2-hydroxypinan-3-one was prepared by the method of H. Schmidt, Chem. Ber. 1960, 93, 2485.
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(1960)
Chem. Ber.
, vol.93
, pp. 2485
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Schmidt, H.1
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