Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5270847 | Tetrahedron Letters | 2010 | 4 Pages |
After the protection of two α-carbons of the dibenzothiophene moiety in triphenylenothiophene 1 by trimethylsilyl groups, the resulting compound 4 reacted with butyllithium followed by dichlorodimethylsilane to afford 10H-silolo[2′,3′,4′,5′:4,5]triphenyleno[1,12-bcd]thiophene 8, which reacted with butyllithium followed by dichlorodimethylsilane to afford novel heterasumanene 11. Using dichlorodimethylstannane instead of dichlorodimethylsilane afforded heterasumanene 12, which is the first example of a heterasumanene having three different heteroatom functionalities.
Graphical abstractNovel heterasumanenes were successfully synthesized by stepwise heteroatom functionalization from triphenyleno[1,12-bcd]thiophene.Figure optionsDownload full-size imageDownload as PowerPoint slide