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letter
. 2016 Jun 22;12:1302–1308. doi: 10.3762/bjoc.12.122

Table 4.

The AuCl3-catalyzed iodination of tetraphenylene (1).

graphic file with name Beilstein_J_Org_Chem-12-1302-i004.jpg

Entry NIS (equiv) T (°C) t (h) Yielda (%)

1 1.0 rt 12 18
2 1.0 60 12 32
3 1.0 80 12 30
4 2.0 60 12 80 (78)b
5 2.0 60 6 72
6 2.0 60 16 52

aThe yields were determined by 1H NMR analysis of the crude products using CH2Br2 as the internal standard. bIsolated yields based on tetraphenylene (1).