The author of 《Transition-metal-free carbonylation of aryl halides with arylboronic acids by utilizing stoichiometric CHCl3 as the carbon monoxide-precursor》 were Xu, Fangning; Li, Dan; Han, Wei. And the article was published in Green Chemistry in 2019. Application of 529-28-2 The author mentioned the following in the article:
Under transition-metal-free conditions, carbonylative Suzuki couplings of aryl halides with arylboronic acid using stoichiometric CHCl3 as the carbonyl source was developed. The simple, efficient and environmentally benign method was successfully applied to the synthesis of fenofibric acid, naphthyl phenstatin and carbon-13 labeled biaryl ketone.1-Iodo-2-methoxybenzene(cas: 529-28-2Application of 529-28-2) was used in this study.
1-Iodo-2-methoxybenzene(cas: 529-28-2) participates in palladium catalyzed enantioselective Heck arylation of 2,3-dihydrofuran in the presence of chiral ionic liquids containing L-prolinate and L-lactate anions and non-chiral quaternary ammonium cations.Application of 529-28-2
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem