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more..
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b) Dawson, M. J.; Farthing, J. E.; Marshall, P. S.; Middleton, R. F.; O'Neill, M. J.; Shuttleworth, A.; Stylli, C.; Tait, R. M.; Taylor, P. M.; Wildman, H. G.; Buss, A. D.; Langley, D.; Hayes, M. V. J. Antibiot. 1992, 45, 639.
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0028841895
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and references therein
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Bergstrom, J. D.; Dufresne, C.; Bills, G. F.; Nallin-Omstead, M.; Byrne, K. Ann. Rev. Microbiol. 1995, 49, 607. (and references therein).
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Nicolaou, K. C.; Yue, E. W.; Naniwa, Y.; De Riccardis, F.; Nadin, A.; Leresche, J. E.; La Greca, S.; Yang, Z. Angew. Chem. Int. Ed. Engl. 1994, 33, 2184.
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0342661459
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Evans has observed a similar trend in the energies of ketals of this type. See reference 4b
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Evans has observed a similar trend in the energies of ketals of this type. See reference 4b.
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10
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0006064881
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2, TEA. 5. O,2-dianion of allyl alcohol, THF, -78°C. Complete experimental details are published elsewhere. See Hegde, S. G. and Myles, D. C. submitted. The preparation of the O,2-dianion of allyl alcohol was originally reported by Corey (Corey, E. J.; Widiger, G. N.; J. Org. Chem., 1975, 40, 2975). We have found that the reliability with which the dianion is formed is greatly enhanced by carrying out the deprotonation with methylmagnesium bromide prior to halogen metal exchange with tert-butyllithium. Hegde, S. G.; Myles, D. C.Syn. Commun., 1996, in press.
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Widiger, G.N.2
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0342755087
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in press
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2, TEA. 5. O,2-dianion of allyl alcohol, THF, -78°C. Complete experimental details are published elsewhere. See Hegde, S. G. and Myles, D. C. submitted. The preparation of the O,2-dianion of allyl alcohol was originally reported by Corey (Corey, E. J.; Widiger, G. N.; J. Org. Chem., 1975, 40, 2975). We have found that the reliability with which the dianion is formed is greatly enhanced by carrying out the deprotonation with methylmagnesium bromide prior to halogen metal exchange with tert-butyllithium. Hegde, S. G.; Myles, D. C.Syn. Commun., 1996, in press.
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0342661458
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submitted
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Conditions for this oxidation are published elsewhere. Hegde, S. G.; Myles D. C. submitted.
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Hegde, S.G.1
Myles, D.C.2
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15
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0343967512
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Ph.D., Director
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NMR experiments were conducted at the UCLA Chemical Instrumentation Facility, J. Strouse, Ph.D., Director.
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0026493653
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Dufresne, C.; Wilson, K. E.; Zink, D.; Smith, J.; Bergstrom, J. D.; Kurtz, M.; Rew, D.; Nallin, M.; Jenkins, R.; Bartizal, K.; Trainor, C.; Bills, G.; Meinz, M.; Huang, L.; Onishi, J.; Milligan, J.; Mojena, M.; Pelaez, F. Tetrahedron 1992, 48, 10221.
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