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For some reviews on β-lactam antibiotics, see: (a) Chemistry and Biology of β-Lactam Antibiotics; Morin, R. B.; Gorman, M., Eds.; Academic Press: New York, 1982; Vol. 1-3; (b) Recent Advances in the Chemistry of β-Lactam Antibiotics; Brown, A. G.; Roberts, S. M., Eds.; The Royal Society of Chemistry, Burling House: London, 1984; (c) The Chemistry of β-Lactams; Page, M. I., Ed.; Chapman and Hall: London, 1992.
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Morin, R.B.1
Gorman, M.2
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0003808393
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The Royal Society of Chemistry, Burling House: London
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For some reviews on β-lactam antibiotics, see: (a) Chemistry and Biology of β-Lactam Antibiotics; Morin, R. B.; Gorman, M., Eds.; Academic Press: New York, 1982; Vol. 1-3; (b) Recent Advances in the Chemistry of β-Lactam Antibiotics; Brown, A. G.; Roberts, S. M., Eds.; The Royal Society of Chemistry, Burling House: London, 1984; (c) The Chemistry of β-Lactams; Page, M. I., Ed.; Chapman and Hall: London, 1992.
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Recent Advances in the Chemistry of β-Lactam Antibiotics
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Brown, A.G.1
Roberts, S.M.2
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0004030275
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Chapman and Hall: London
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For some reviews on β-lactam antibiotics, see: (a) Chemistry and Biology of β-Lactam Antibiotics; Morin, R. B.; Gorman, M., Eds.; Academic Press: New York, 1982; Vol. 1-3; (b) Recent Advances in the Chemistry of β-Lactam Antibiotics; Brown, A. G.; Roberts, S. M., Eds.; The Royal Society of Chemistry, Burling House: London, 1984; (c) The Chemistry of β-Lactams; Page, M. I., Ed.; Chapman and Hall: London, 1992.
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The Chemistry of β-Lactams
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Page, M.I.1
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Palomo C., Cossio F.P., Cuevas C., Odriozola J.M., Ontoria J.M. Tetrahedron Lett. 33:1992;4827.
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Tetrahedron Lett.
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Palomo, C.1
Cossio, F.P.2
Cuevas, C.3
Odriozola, J.M.4
Ontoria, J.M.5
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Palomo C., Aizpurus J.M., Garcia J.M., Iturburu M., Odriozola J.M. J. Org. Chem. 59:1994;5184.
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Palomo, C.1
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Garcia, J.M.3
Iturburu, M.4
Odriozola, J.M.5
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14
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0028914757
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For the nucleophilic ring opening of monosubstituted 2-azetidinone with carbanions, see: (a) Baldwin, J. E.; Adlington, R. M.; Russel, A. T.; Smith, M. L. Tetrahedron 1995, 51, 4733; (b) Baldwin, J. E.; Adlington, R. M.; Godfrey, C. R. A.; Gollins, D. W.; Smith, M. L.; Russel, A. T. Synlett 1993, 51.
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Tetrahedron
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Baldwin, J.E.1
Adlington, R.M.2
Russel, A.T.3
Smith, M.L.4
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15
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85060086983
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For the nucleophilic ring opening of monosubstituted 2-azetidinone with carbanions, see: (a) Baldwin, J. E.; Adlington, R. M.; Russel, A. T.; Smith, M. L. Tetrahedron 1995, 51, 4733; (b) Baldwin, J. E.; Adlington, R. M.; Godfrey, C. R. A.; Gollins, D. W.; Smith, M. L.; Russel, A. T. Synlett 1993, 51.
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Synlett
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Baldwin, J.E.1
Adlington, R.M.2
Godfrey, C.R.A.3
Gollins, D.W.4
Smith, M.L.5
Russel, A.T.6
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16
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0032506676
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By now, only one example of HWE olefination of β-ketophosphonates derived from amino acid with aldehyde was reported.
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By now, only one example of HWE olefination of β-ketophosphonates derived from amino acid with aldehyde was reported. Werner R.M., Williams L.M., Davis J.T. Tetrahedron Lett. 39:1998;9135.
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Werner, R.M.1
Williams, L.M.2
Davis, J.T.3
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22
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0012004415
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note
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+, 2), 594 (100), 494 (43), 354 (52%).
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