246230-86-4Relevant articles and documents
Synthesis of 3-Iodobenzofurans by Electrophilic Cyclization under Solventless Conditions in a Ball Mill
Mantovani, Anderson C.,Hernández, José G.,Bolm, Carsten
, p. 2458 - 2461 (2018)
Under mechanochemical conditions, electrophilic cyclizations of 2-alkynylanisoles provide 3-iodobenzofurans in the absence of a solvent. Equimolar amounts of iodine are sufficient for achieving good yields. The eco-friendly reaction conditions are mild, and various functional groups are tolerated.
New Access to Six-Membered Phosphacycle Annulated Polyaromatic Ring System
Si, Erbing,Zhao, Peng,Wang, Lili,Duan, Zheng,Mathey, Fran?ois
supporting information, p. 697 - 701 (2020/02/11)
A facile Ag-catalyzed intramolecular C–P bond formation reaction from easily accessible phosphine oxides has been developed. Several new heteroatoms fused π-conjugated molecules were synthesized from this procedure with their structures confirmed by X-ray
A concise approach for the synthesis of 3-iodoindoles and 3-iodobenzo[b]furans via Ph3P-catalyzed iodocyclization
Li, Yin-Long,Li, Jian,Yu, Sheng-Nan,Wang, Ji-Bo,Yu, Yan-Min,Deng, Jun
, p. 8271 - 8277 (2015/10/05)
A variety of 3-iodoindole and 3-iodobenzo[b]furan derivatives were conveniently prepared from the corresponding 2-alkynylanilines and 2-alkynylphenols through Ph3P-catalyzed iodocyclization in the presence of N-iodosuccinimide (NIS). This proto