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0028111884
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Blackie Academic & Professional: New York
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Overviews of β-lactam antibiotics are presented in the following: (a) The Chemistry of β-Lactams; Page, M. I., Ed.; Blackie Academic & Professional: New York, 1992. (b) The Organic Chemistry of β-Lactams; Georg, G. I., Ed.; VCH Press: New York, 1993. (c) Samarendra, C. I.; Maiti, N.; Micetich, R. G.; Daneshtalab, M.; Atchison, K.; Phillips, O. A.; Kunugita, C. J. Antibiot. 1994, 47, 1030 and references therein.
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The Chemistry of β-Lactams
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Page, M.I.1
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2
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0028111884
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VCH Press: New York
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Overviews of β-lactam antibiotics are presented in the following: (a) The Chemistry of β-Lactams; Page, M. I., Ed.; Blackie Academic & Professional: New York, 1992. (b) The Organic Chemistry of β-Lactams; Georg, G. I., Ed.; VCH Press: New York, 1993. (c) Samarendra, C. I.; Maiti, N.; Micetich, R. G.; Daneshtalab, M.; Atchison, K.; Phillips, O. A.; Kunugita, C. J. Antibiot. 1994, 47, 1030 and references therein.
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The Organic Chemistry of β-Lactams
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Georg, G.I.1
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3
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0028111884
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and references therein
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Overviews of β-lactam antibiotics are presented in the following: (a) The Chemistry of β-Lactams; Page, M. I., Ed.; Blackie Academic & Professional: New York, 1992. (b) The Organic Chemistry of β-Lactams; Georg, G. I., Ed.; VCH Press: New York, 1993. (c) Samarendra, C. I.; Maiti, N.; Micetich, R. G.; Daneshtalab, M.; Atchison, K.; Phillips, O. A.; Kunugita, C. J. Antibiot. 1994, 47, 1030 and references therein.
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Samarendra, C.I.1
Maiti, N.2
Micetich, R.G.3
Daneshtalab, M.4
Atchison, K.5
Phillips, O.A.6
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(a) Hornback, W. J.; Munroe, J. E.; Counter, F. T. J. Antibiot. 1994, 47, 1052.
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Novel Methods for the Construction of the β-Lactam Ring
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Georg, G. I., Ed.; VCH Press: New York
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Ternansky, R. J.; Morin, J. M., Jr. Novel Methods for the Construction of the β-Lactam Ring. In The Organic Chemistry of β-Lactams; Georg, G. I., Ed.; VCH Press: New York, 1993; p 257.
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Initial observation of this effect was made by N. Atanes of this laboratory
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Initial observation of this effect was made by N. Atanes of this laboratory.
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13
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2 are presented in the following: Provot, O.; Celerier, J. P.; Petit, H.; Lhommet, G. Synthesis 1993, 69 and references therein.
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For a related example, see: Yamashita, H.; Minami, N.; Sakakibara, K.; Kobayashi, S.; Ohno, M. Chem. Pharm. Bull. 1988, 36, 469.
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44
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note
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Ketone 3 was recrystallized from EtOAc prior to use in order to remove any traces of the α,β-unsaturated ketone 4. The presence of as little as 4% of conjugated ketone 4 in a sample of ketone 3 produces significantly lower yields of diol.
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