Electron transfer processes. 53. Homolytic alkylation of enamines by

bridgehead substituents on the fenestrane framework. Preliminary force-field calculations suggest that the. “planoid” distortions at the centralca...
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J. Org. Chem. 1991,56,3415-3479 The results presented here show that a range of fenestranes with fourfold bridgehead substitution has become synthetically accessible. %e NMR data clearly reveal that the barrier to conformational interconversion, and thus the unfavorable steric and, probably, dipolar interactions, increase in the order F, OH