- 2,5,6-Trisubstituted N-Methylindoles from Site-Selective Suzuki-Miyaura Cross-Coupling, Twofold Heck and 6 pi-Electrocyclization-Dehydrogenation Reactions of 2,3,5-Tribromo-N-methylpyrrole
[作者:TOGUEM SERGEMITHERAND TENGHO; LANGER PETER,期刊:SYNLETT, 页码:513-516 , 文章类型: Article,,卷期:2011年-4]
- Site-selective Suzuki-Miyaura reactions of 2,3,5-tribromo-N-methylpyrrole afforded 5-aryl-2,3-dibromo-N-methylpyrroles. These products were transformed into 2,5,6-trisubstituted N-methylindoles by twofold Heck reactions ...
- Electrophilic Cyclization of Buta-1,3-diynylarenes: Synthesis of Precursors of (Z)-3-Ene-1,5-diyne Systems Fused to Heterocycles
[作者:DANILKINA NATALIA A; BRAESE STEFAN; BALOVA IRINA A,期刊:SYNLETT, 页码:517-520 , 文章类型: Article,,卷期:2011年-4]
- A simple, convenient, and promising strategy for the synthesis of 2-ethynyl-3-iodo-benzothiophenes, -benzofurans, and -indoles based on electrophilic cyclization of easily available ortho-functionalized (buta-1,3-diynyl)...
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