Competition between planar and central chiral control elements in nucleophilic addition to ferrocenyl imine derivatives
Literature Information
Kévin M. Joly, Claire Wilson, Alexander J. Blake, James H. R. Tucker, Christopher J. Moody
Planar chirality associated with the ferrocene in ferrocenyl oximes and hydrazones bearing chiral auxiliaries effectively competes with or overrides the normally excellent stereocontrol afforded by the auxiliary in determining the diastereoselectivity of addition to the CN bond.
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Chemical Communications

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![2,6-Di(thiophen-2-yl)dithieno[3,2-b:2',3'-d]thiophene structure 2,6-Di(thiophen-2-yl)dithieno[3,2-b:2',3'-d]thiophene structure](https://static.chemtradehub.com/structs/910/910788-24-8-5b70.webp)

