Copper‐Mediated Diamination of Arylboronic Acids for the Synthesis of 2‐Aryl Benzimidazoles Using Trimethylsilyl Azide as the Amino Sources with Aldehydes-Reference-Cited by-同舟云学术

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Copper‐Mediated Diamination of Arylboronic Acids for the Synthesis of 2‐Aryl Benzimidazoles Using Trimethylsilyl Azide as the Amino Sources with Aldehydes

Published:2020-07-24 Issue:16 Volume:362 Page:3442-3446
ISSN:1615-4150
Container-title:Advanced Synthesis & Catalysis
language:en
Short-container-title:Adv. Synth. Catal.

Author:

Xie Zeqiang¹,Zhou Fengtao¹,Ding Ke¹

Affiliation:

1. International Cooperative Laboratory of Traditional Chinese Medicine Modernization and Innovative Drug Discovery of Chinese Ministry of Education (MOE)Guangzhou City Key Laboratory of Precision Chemical Drug DevelopmentSchool of PharmacyJinan University 601 Huangpu Avenue West Guangzhou 510632 People's Republic of China

Funder

China Postdoctoral Science Foundation

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202000385

Reference65 articles.

1. A new stereospecific cross-coupling by the palladium-catalyzed reaction of 1-alkenylboranes with 1-alkenyl or 1-alkynyl halides

2.

3. New N- and O-arylations with phenylboronic acids and cupric acetate

4. Synthesis of diaryl ethers through the copper-promoted arylation of phenols with arylboronic acids. An expedient synthesis of thyroxine

5. New aryl/heteroaryl CN bond cross-coupling reactions via arylboronic acid/cupric acetate arylation

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