Xantphos‐ligated palladium dithiolates: An unprecedented and convenient catalyst for the carbonylative Suzuki–Miyaura cross‐coupling reaction with high turnover number and turnover frequency-Reference-Cited by-同舟云学术

Xantphos‐ligated palladium dithiolates: An unprecedented and convenient catalyst for the carbonylative Suzuki–Miyaura cross‐coupling reaction with high turnover number and turnover frequency

Published:2019-11-13 Issue:1 Volume:34 Page:
ISSN:0268-2605
Container-title:Applied Organometallic Chemistry
language:en
Short-container-title:Appl Organometal Chem

Author:

Gaikwad Vinayak V.¹^ORCID,Mane Pravin A.²,Dey Sandip²³^ORCID,Bhanage Bhalchandra M.¹^ORCID

Affiliation:

1. Department of ChemistryInstitute of Chemical Technology Nathalal Parekh Marg, Matunga Mumbai 400019 India

2. Chemistry DivisionBhabha Atomic Research Centre Mumbai 400085 India

3. Training School ComplexHomi Bhabha National Institute Mumbai 400094 India

Publisher

Wiley

Subject

Inorganic Chemistry,General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/aoc.5255

Reference61 articles.

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

2. Current technologies for the production of (S)-ketoprofen: Process perspective

3. Analysis of sofalcone in human plasma by high performance liquid chromatography

4. Efficient Light Emitters in the Solid State: Synthesis, Aggregation-Induced Emission, Electroluminescence, and Sensory Properties of Luminogens with Benzene Cores and Multiple Triarylvinyl Peripherals

5. Synthesis of aromatic poly(ether ketone)s bearing optically active macrocycles through Suzuki coupling polymerization

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