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3/MeOH resulted in a 1:1 mixture of i and ii. Thus, the pinacol product differs in the configuration of the enolizable carbon, as expected from the assigned configurations of 29b and 2a if the pinacol rearrangement occurs with stereospecific hydride migration to the backside of the protonated tertiary hydroxyl group.
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(b) Osmylation syn to allylic N-H is known in an amide example, but this selectivity may be influenced by additional factors: King, S. B.; Ganem, B. J. Am. Chem. Soc. 1991, 113, 5089 and references therein.
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For leading references to syn direction by other allylic heteroatoms, see ref 5c. (c) Krysan, D. J.; Rockway, T. W.; Haight, A. R. Tetrahedron: Asymmetry 1994, 5, 625 and references therein. (d) Reetz, M. T.; Strack, T. J.; Mutulis, F.; Goddard, R. Tetrahedron Lett. 1996, 37, 9293. Paz, M. M.; Sardina, F. J. J. Org. Chem. 1993, 58, 6990. Hauser, F. M.; Ellenberger, S. R. J. Am. Chem. Soc. 1984, 106, 2458. Hauser, F. M.; Rhee, R. P. J. Org. Chem. 1981, 46, 227.
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