Stereoselective acyclic enolate formation via conjugate reduction: correlation with enone conformational preferences

AR Chamberlin, SH Reich

Index: Chamberlin, A. Richard; Reich, Siegfried H. Journal of the American Chemical Society, 1985 , vol. 107, # 5 p. 1440 - 1441

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Citation Number: 40

Abstract

Figure 1. 3-21G Molecular structures. Bond lengths in A, angles in degrees. energy increases monotonically upon rotation from pyramidal to planar. In the more stable form with M= Si the two Si-Si distances are very similar to those in disilane at a comparable level of theory, 2 with the base bond being slightly longer than the internal bond. For M= C, the Si-C bond is slightly shorter than that in methylsilane, while the Si-Si bond is much shorter than ...