A phosphine-free, atom-efficient cross-coupling reaction of triorganoindiums with acyl chlorides catalyzed by immobilization of palladium(0) in MCM-41-Reference-Cited by-同舟云学术

A phosphine-free, atom-efficient cross-coupling reaction of triorganoindiums with acyl chlorides catalyzed by immobilization of palladium(0) in MCM-41

Published:2017 Issue:67 Volume:7 Page:42570-42578
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Miao Jiankang¹²³⁴⁵,Huang Bin¹²³⁴⁵,Liu Haiyi¹²³⁴⁵,Cai Mingzhong¹²³⁴⁵^ORCID

Affiliation:

1. Key Laboratory of Functional Small Organic Molecules

2. Ministry of Education

3. College of Chemistry & Chemical Engineering

4. Jiangxi Normal University

5. Nanchang 330022

Abstract

The phosphine-free, atom-efficient cross-coupling of triorganoindiums with acyl chlorides has been achieved using a recyclable MCM-41-immobilized palladium(0)–Schiff base complex.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/RA/C7RA08355F

Reference85 articles.

1. A new efficient synthesis of pyridines

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3. Addition of Grignard Reagents to Aryl Acid Chlorides: An Efficient Synthesis of Aryl Ketones

4. Disproportionation of diarylmethanol derivatives by using supercritical water

5. Diverse Strategies toward Indenol and Fulvene Derivatives: Rh-Catalyzed C−H Activation of Aryl Ketones Followed by Coupling with Internal Alkynes

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