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| Supporting Information File 1: Detailed experimental procedures and copies of 1H and 13C NMR spectra of all synthesised compounds. | ||
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Cite the Following Article
Palladium-catalysed cross-coupling reaction of ultra-stabilised 2-aryl-1,3-dihydro-1H-benzo[d]1,3,2-diazaborole compounds with aryl bromides: A direct protocol for the preparation of unsymmetrical biaryls
Siphamandla Sithebe and Ross S. Robinson
Beilstein J. Org. Chem. 2014, 10, 1107–1113.
https://doi.org/10.3762/bjoc.10.109
How to Cite
Sithebe, S.; Robinson, R. S. Beilstein J. Org. Chem. 2014, 10, 1107–1113. doi:10.3762/bjoc.10.109
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- Stewart, S. G.; Smith, J. A.; Condie, R. Comprehensive Heterocyclic Chemistry IV - Three or Four Heteroatoms Including at Least One Boron. Comprehensive Heterocyclic Chemistry IV; Elsevier, 2022; pp 444–476. doi:10.1016/b978-0-12-818655-8.00120-7
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- Davies, G.; Molander, G. A. Synthesis of Functionalized 1,3,2-Benzodiazaborole Cores Using Bench-Stable Components. The Journal of organic chemistry 2016, 81, 3771–3779. doi:10.1021/acs.joc.6b00435
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