Iron-catalyzed cross-coupling of arylboronic acids with unactivated <i>N</i>-heterocycles and quinones under microwave heating

نویسندگان

چکیده

The iron-catalyzed direct arylation of a variety N-heteroarenes, quinones, and hydroquinones with arylboronic acids is investigated under microwave heating. reaction proceeds at 70 °C air using K 2 S O 8 as an oxidant FeSO 4 catalyst. Under heating, times decreased 14- to 115-fold. Reaction scope N-heteroarenes quinones comparable or slightly expanded when compared previous reports, but the acid utility was limited due previously unobserved hydroxydeboronation.

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Palladium-catalyzed decarboxylative coupling of aromatic acids with aryl halides or unactivated arenes using microwave heating.

Microwave heating greatly accelerates Pd-catalyzed decarboxylative coupling of aromatic acids and aryl iodides, and allows the coupling of benzoic acids with unactivated arenes.

متن کامل

Suzuki-Miyaura cross-coupling reaction catalyzed using highly efficient CN-dimeric ortho-palladated complex under microwave irradiation and conventional heating

Suzuki cross-coupling reaction of different aryl halides with arylboronic acids was successfully carried out in methanol using ortho-palladated complex of 2-methoxyphenethylamine. All substrates afforded the corresponding products in good to high yields in the presence of low amounts of this complex as efficient and active catalyst. Application of microwave irradiation improved the yields of th...

متن کامل

Suzuki-Miyaura cross-coupling reaction catalyzed using highly efficient CN-dimeric ortho-palladated complex under microwave irradiation and conventional heating

Suzuki cross-coupling reaction of different aryl halides with arylboronic acids was successfully carried out in methanol using ortho-palladated complex of 2-methoxyphenethylamine. All substrates afforded the corresponding products in good to high yields in the presence of low amounts of this complex as efficient and active catalyst. Application of microwave irradiation improved the yields of th...

متن کامل

Palladium-catalyzed decarboxylative cross-coupling of alkynyl carboxylic acids with arylboronic acids.

A highly efficient and mild palladium-catalyzed decarboxylative cross-coupling of aryl boronic acids and alkynyl carboxylic acids for the synthesis of unsymmetrical substituted alkynes is described for the first time.

متن کامل

The coupling of arylboronic acids with nitroarenes catalyzed by rhodium.

The coupling of arylboronic acids with electron-deficient nitroarenes was realized for the first time by using a rhodium(I) catalyst under an air atmosphere, achieving unsymmetrical diaryl ethers with yields ranging from poor to good. From a deuterium labeling experiment, the oxygen atom is derived from ambient water. The efficiency of this reaction was demonstrated by its compatibility with fl...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Canadian Journal of Chemistry

سال: 2021

ISSN: ['0008-4042', '1480-3291']

DOI: https://doi.org/10.1139/cjc-2020-0339