2008
DOI: 10.1016/j.jorganchem.2007.09.034
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Wide bite angle diphosphine rhodium complexes: Synthesis, structure, and catalytic 1,4-addition of arylboronic acids to enones

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Cited by 16 publications
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“…(Scheme ). Resonances at 3.07 ppm (major isomer) and 3.02 ppm (minor isomer) in the 1 H NMR spectrum are attributable to the −OC H 3 substituent of 1a remaining intact in 23a , assigned as a diphosphine Rh­(Cl)­(CO) species with an IR stretch assigned to Rh–CO (ν CO = 1957 cm –1 ) comparable to those reported in the literature for similar compounds. , Heating a solution of 23a in a sealed J. Young tube affords the new compound 24a with a new resonance observed by 31 P NMR spectroscopy (43.34 ppm) and an IR stretch (ν CO = 1942 cm –1 ) comparable to those of previously reported phenoxide diphosphine RhCl species .…”
Section: Resultssupporting
confidence: 70%
“…(Scheme ). Resonances at 3.07 ppm (major isomer) and 3.02 ppm (minor isomer) in the 1 H NMR spectrum are attributable to the −OC H 3 substituent of 1a remaining intact in 23a , assigned as a diphosphine Rh­(Cl)­(CO) species with an IR stretch assigned to Rh–CO (ν CO = 1957 cm –1 ) comparable to those reported in the literature for similar compounds. , Heating a solution of 23a in a sealed J. Young tube affords the new compound 24a with a new resonance observed by 31 P NMR spectroscopy (43.34 ppm) and an IR stretch (ν CO = 1942 cm –1 ) comparable to those of previously reported phenoxide diphosphine RhCl species .…”
Section: Resultssupporting
confidence: 70%