@article{fed8fc76a83f4f95bff11dbdb450bc3e,
title = "Decarbonylative Synthesis of Aryl Nitriles from Aromatic Esters and Organocyanides by a Nickel Catalyst",
abstract = "A decarbonylative cyanation of aromatic esters with aminoacetonitriles in the presence of a nickel catalyst was developed. The key to this reaction was the use of a thiophene-based diphosphine ligand, dcypt, permitting the synthesis of aryl nitrile without the generation of stoichiometric metal- or halogen-containing chemical wastes. A wide range of aromatic esters, including hetarenes and pharmaceutical molecules, can be converted into aryl nitriles. ",
keywords = "aminoacetonitriles, aromatic esters, coupling reaction, cyanation, nickel catalysis",
author = "Keiichiro Iizumi and Kurosawa, {Miki B.} and Ryota Isshiki and Kei Muto and Junichiro Yamaguchi",
note = "Funding Information: This work was supported by JSPS KAKENHI Grant Number JP19H02726 (to J.Y.), JP20H04829 (hybrid catalysis), and JP19K15573 (to K.M.).JapanSocieyforhePromotionofScience(JP19H02726)JapanSocietyfrthePomoionofScience(JP19K15573) Publisher Copyright: {\textcopyright} 2020. Thieme. All rights reserved.",
year = "2021",
month = sep,
day = "16",
doi = "10.1055/s-0040-1705943",
language = "English",
volume = "32",
pages = "1555--1559",
journal = "Synlett",
issn = "0936-5214",
publisher = "Georg Thieme Verlag",
number = "15",
}