Title of article :
An efficient protocol for synthesizing dibenzodithiapentalenes
Author/Authors :
Jepsen، نويسنده , , Tue Heesgaard and Larsen، نويسنده , , Mogens and Jّrgensen، نويسنده , , Morten and Nielsen، نويسنده , , Mogens Brّndsted، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2011
Pages :
3
From page :
4045
To page :
4047
Abstract :
Two new scalable methods for the synthesis of dibenzo[bc,fg]dithiapentalene (2) (DPP) are reported starting from either 1-bromo-3-fluoro-2-iodobenzene over four steps in 57% yield or from THP-protected 3-fluorothiophenol over three steps in 43% yield. Attempts to prepare dibenzodioxapentalene (15) using similar conditions were unsuccessful. Instead, we observed the formation of a macrocyclic dimeric product 16. Fluorine–hydrogen bond interactions were observed by NMR in the F/SH- and F/OH-substituted dibenzothiophene and dibenzofuran intermediates.
Keywords :
nucleophilic aromatic substitution , Fluorine–hydrogen bonding , 4]dithiapentalene , Dibenzofuran
Journal title :
Tetrahedron Letters
Serial Year :
2011
Journal title :
Tetrahedron Letters
Record number :
1878904
Link To Document :
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