Palladacycle-catalyzed Suzuki–Miyaura reaction of aryl/heteroaryl halides with MIDA boronates in EtOH/H2O or H2O-Reference-Cited by-同舟云学术

Palladacycle-catalyzed Suzuki–Miyaura reaction of aryl/heteroaryl halides with MIDA boronates in EtOH/H2O or H2O

Published:2014 Issue:68 Volume:4 Page:36262-36266
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Li Yabo¹²³⁴⁵,Wang Jingran¹²³⁴⁵,Wang Zhiwei¹²³⁴⁵,Huang Mengmeng¹²³⁴⁵,Yan Beiqi¹²³⁴⁵,Cui Xiuling¹²³⁴⁵,Wu Yusheng¹²³⁴⁵,Wu Yangjie¹²³⁴⁵

Affiliation:

1. College of Chemistry and Molecular Engineering

2. Henan Key Laboratory of Chemical Biology and Organic Chemistry

3. Key Laboratory of Applied Chemistry of Henan Universities

4. Zhengzhou University

5. Zhengzhou, P. R. China

Abstract

With good to excellent yields, a series of mono- or diheteroaryl compounds were synthesized via the palladacycle-catalyzed Suzuki–Miyaura reaction of various N-methyliminodiacetic acid (MIDA) boronates with aryl/heteroaryl halides in EtOH/H₂O or H₂O.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA07486F

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