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Hydride reduction: (a)
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Hydride reduction: (a) Comins, D. L.; Hong, H.; Salvador, J. M. J. Org. Chem. 1991, 56, 7197.
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Comins, D.L.1
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4
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85022826017
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(b) See ref lb. Alkyl nucleophiles: Organocerium reagents undergo preferentially 1,2-addition. Unpublished results.
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(b) See ref lb. Alkyl nucleophiles: Organocerium reagents undergo preferentially 1,2-addition. Comins, D. L.; Bieda, K.; Joseph, S. P. Unpublished results.
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Comins, D.L.1
Bieda, K.2
Joseph, S.P.3
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7
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(1,3) strain, see: (a)
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(1,3) strain, see: (a) Hoffman, R. W. Chem. Rev. 1989, 89, 1841-1860.
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Also see:
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Also see: Beckwith, A. L. J.; Joseph, S. P.; Mayadunne, R. T. A. J. Org. Chem. 1993, 58, 4198.
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Beckwith, A.L.J.1
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Mayadunne, R.T.A.3
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14
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0024447486
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Chiral piperidines have been prepared from N-alkyl-2,3-dihydro-4-pyridones; see: (a)
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Chiral piperidines have been prepared from N-alkyl-2,3-dihydro-4-pyridones; see: (a) Pfrengle, W.; Kunz, H. J. Org. Chem. 1989, 54, 4261.
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Waldmann, H.; Braun, M.; Drager, M. Angew. Chem., Int. Ed. Engl. 1990, 29, 1468.
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Hattori, K.; Yamamoto, H. J. Org. Chem. 1992, 57, 3264 and references cited therein.
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For reviews on dihydropyridines, see: Sausins, A.; Duburs, G. Heterocycles 1988, 27, 291. Also see: Comins, D. L.; O'Connor, S. Adv. Heterocycl. Chem. 1988, 44, 199.
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For reviews on dihydropyridines, see: Stout, D. M.; Meyers, A. I. Chem. Rev. 1982, 82, 223. Sausins, A.; Duburs, G. Heterocycles 1988, 27, 291. Also see: Comins, D. L.; O'Connor, S. Adv. Heterocycl. Chem. 1988, 44, 199.
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