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. Author manuscript; available in PMC: 2013 Jan 14.
Published in final edited form as: Chem Commun (Camb). 2011 Nov 24;48(4):609–611. doi: 10.1039/c1cc15880e

Table 1.

Optimization of ligand for the coupling of 7 with bromobenzenea

graphic file with name nihms366656u1.jpg
Entry Ligand Yieldb
1 graphic file with name nihms366656t1.jpg S-Phos 84% (75%)
2 graphic file with name nihms366656t2.jpg RuPhos 76%
3 graphic file with name nihms366656t3.jpg Me-Phos 31%
4 graphic file with name nihms366656t4.jpg Dave-Phos 12%
5 graphic file with name nihms366656t5.jpg Brett-Phos 47%
6 graphic file with name nihms366656t6.jpg Dpe-Phos 30%
a

Conditions: 1.0 equiv 7, 2.0 equiv PhBr, 2.0 equiv NaOtBu, 2 mol % Pd2(dba)3, 4 mol % ligand, toluene (0.25 M), 110 °C.

b

Yields were determined by 1H NMR analysis of crude reaction mixtures using phenanthrene as an internal standard. The yield in parentheses is an isolated yield of pure product.