Article ID Journal Published Year Pages File Type
5270847 Tetrahedron Letters 2010 4 Pages PDF
Abstract

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

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry