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. 2016 Aug 16;12:1851–1862. doi: 10.3762/bjoc.12.174

Table 3.

Comparing the reactivity of 6-iodo-THQ 21 and 6-bromo-THQ 26 in a typical Suzuki reaction with boronic ester 27 to give biaryl 28.

graphic file with name Beilstein_J_Org_Chem-12-1851-i002.jpg

THQ Halide Conversion of starting materiala Isolated yield of 28

21 I 100% 68%
26 Br 56% N/Ab

aConversion of the starting THQs 21/26 to the coupling product 28 was estimated by comparing the integrals of the CH2 adjacent to the nitrogen (the 2-position) in the crude 1H NMR spectrum. bNot isolated.