Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1315053 | Journal of Fluorine Chemistry | 2010 | 5 Pages |
Abstract
A chiral 2-naphthylferrocenylcopper heteroaggregate (2) was prepared in high yield by reaction of (Sp-2-naphthylferrocenyl)trimethyltin with (C6F5Cu)4 and fully characterized by multinuclear NMR, single crystal X-ray diffraction, and elemental analysis. The reactivity of 2 toward boron halides was examined. Rearrangement reactions resulted in formation of 1,2-, 1,3-, and 1,1′-disubstituted naphthylferrocenylboranes.
Graphical abstractA chiral 2-naphthylferrocenylcopper heteroaggregate was prepared in high yield by reaction of (Sp-2-naphthylferrocenyl)trimethyltin with (C6F5Cu)4 and its reactivity toward boron halides was examined.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Krishnan Venkatasubbaiah, Michael Bolte, Frieder Jäkle,