A Pd–Sn heterobimetallic catalyst for carbonylative Suzuki, Sonogashira and aminocarbonylation reactions using chloroform as a CO surrogate-Reference-Cited by-同舟云学术

A Pd–Sn heterobimetallic catalyst for carbonylative Suzuki, Sonogashira and aminocarbonylation reactions using chloroform as a CO surrogate

Published:2023 Issue:27 Volume:21 Page:5601-5608
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Mohanty Anuradha¹,Nayak Mukesh Kumar¹,Roy Sujit¹^ORCID

Affiliation:

1. Organometallics & Catalysis Laboratory, School of Basic Sciences, Indian Institute of Technology Bhubaneswar, Arugul, Jatani, Khurda 752050, Odisha, India

Abstract

A variety of ketones, amides, and aromatic ynones were synthesized in moderate to good yields in the presence of a heterobimetallic PdCl(PPh3)2SnCl3 catalyst by using chloroform as a CO source in a one-pot fashion.

Funder

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00676J

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5. G. W.Parshall , Homogeneous Catalysis , Wiley - Interprise Publication , New York , 1980

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Aminocarbonylation Reaction Using a Pd–Sn Heterobimetallic Catalyst: Three-Component Coupling for Direct Access of the Amide Functionality;The Journal of Organic Chemistry;2024-01-06

2. Carbon monoxide surrogates for palladium-catalyzed Suzuki-Miyaura and Sonogashira carbonylative cross-coupling reactions;Inorganica Chimica Acta;2023-12