Pd-functionalized MCM-41 nanoporous silica as an efficient and reusable catalyst for promoting organic reactions

RSC Advances ◽  
2015 ◽  
Vol 5 (21) ◽  
pp. 16029-16035 ◽  
Author(s):  
Razieh Nejat ◽  
Ali Reza Mahjoub ◽  
Zahra Hekmatian ◽  
Tahereh Azadbakht
Keyword(s):  
Cross Coupling ◽  
Recyclable Catalyst ◽  
Solvent Free ◽  
Organic Reactions ◽  
Nanoporous Silica ◽  
Reusable Catalyst ◽  
Coupling Reactions ◽  
Cross Coupling Reactions ◽  
Solvent Free Conditions ◽  
Mcm 41

Pd-functionalized MCM-41 nanoporous silica has been explored as an efficient and recyclable catalyst to effect Suzuki and Mizoroki–Heck cross-coupling reactions, under solvent-free conditions.

Withdrawal Notice: Recent Advances in Sonogashira Cross-Coupling Reactions Under Solvent-Free Conditions

2020 ◽  
Vol 24 ◽  
Author(s):  
Teng Wang ◽  
Zongrui Liu ◽  
Songlin Wang ◽  
Esmail Vessally
Keyword(s):  
Organic Chemistry ◽  
Editorial Policy ◽  
Cross Coupling ◽  
Solvent Free ◽  
Coupling Reactions ◽  
Editorial Policies ◽  
Cross Coupling Reactions ◽  
Recent Advances ◽  
Solvent Free Conditions ◽  
Copyright Permission

The article has been withdrawn at the request of editor of the journal Current Organic Chemistry: Bentham Science apologizes to the readers of the journal for any inconvenience this may have caused. The Bentham Editorial Policy on Article Withdrawal can be found at https://benthamscience.com/editorial-policies-main.php BENTHAM SCIENCE DISCLAIMER: It is a condition of publication that manuscripts submitted to this journal have not been published and will not be simultaneously submitted or published elsewhere. Furthermore, any data, illustration, structure or table that has been published elsewhere must be reported, and copyright permission for reproduction must be obtained. Plagiarism is strictly forbidden, and by submitting the article for publication the authors agree that the publishers have the legal right to take appropriate action against the authors, if plagiarism or fabricated information is discovered. By submitting a manuscript, the authors agree that the copyright of their article is transferred to the publishers if and when the article is accepted for publication.

Stannylation of Aryl Halides, Stille Cross-Coupling, and One-Pot, Two-Step Stannylation/Stille Cross-Coupling Reactions under Solvent-Free Conditions

2018 ◽  
Vol 2018 (1) ◽  
pp. 120-125 ◽  
Author(s):  
Pavel S. Gribanov ◽  
Yulia D. Golenko ◽  
Maxim A. Topchiy ◽  
Lidiya I. Minaeva ◽  
Andrey F. Asachenko ◽  
...  
Keyword(s):  
Cross Coupling ◽  
Solvent Free ◽  
Aryl Halides ◽  
Coupling Reactions ◽  
One Pot ◽  
Cross Coupling Reactions ◽  
Solvent Free Conditions

Xylan-type hemicellulose supported palladium nanoparticles: a highly efficient and reusable catalyst for the carbon–carbon coupling reactions

2014 ◽  
Vol 4 (5) ◽  
pp. 1426-1435 ◽  
Author(s):  
Wei Chen ◽  
Lin-xin Zhong ◽  
Xin-wen Peng ◽  
Kun Wang ◽  
Zhi-feng Chen ◽  
...  
Keyword(s):  
Heterogeneous Catalyst ◽  
Palladium Nanoparticles ◽  
Cross Coupling ◽  
Recyclable Catalyst ◽  
Reusable Catalyst ◽  
Coupling Reactions ◽  
Highly Efficient ◽  
Cross Coupling Reactions ◽  
Supported Palladium

A heterogeneous catalyst was prepared by depositing palladium nanoparticles onto xylan-type hemicellulose, which is a kind of renewable biopolymer catalyst, and used as an efficient and recyclable catalyst for the Suzuki, Heck, and Sonogashira cross-coupling reactions.

Bis(NHC)-Pd catalyzed one-pot competitive of C-C*C-C, C-C*C-O, C-C*C-N, and C-O*C-N cross-coupling reactions on an aryl di-halide catalyzed by a homogenous basic ionic liquid (TAIm[OH]) under base-free, ligand-free and solvent-free conditions

2021 ◽  
Author(s):  
Yanfang Zhu ◽  
Guiyang Xu ◽  
Milad Kazemnejadi
Keyword(s):  
Ionic Liquid ◽  
Free Ligand ◽  
Cross Coupling ◽  
Solvent Free ◽  
Coupling Reactions ◽  
One Pot ◽  
Cross Coupling Reactions ◽  
Solvent Free Conditions ◽  
Basic Ionic Liquid ◽  
Ligand Free

Bis(NHC)-Pd-catalyzed competitive asymmetrical C-C*C-C, C-C*C-O, C-C*C-N, O-C*C-N cross-coupling reactions has been performed one-pot in the presence of a new ionic liquid, which plays the roles of solvent, base, and ligand...

Application of a 2-aryl indenylphosphine ligand in the Buchwald–Hartwig cross-coupling reactions of aryl and heteroaryl chlorides under the solvent-free and aqueous conditions

2017 ◽  
Vol 15 (27) ◽  
pp. 5805-5810 ◽  
Author(s):  
Yan Liu ◽  
Jia Yuan ◽  
Zi-Fei Wang ◽  
Si-Hao Zeng ◽  
Meng-Yue Gao ◽  
...  
Keyword(s):  
Catalytic System ◽  
Coupling Reaction ◽  
Cross Coupling ◽  
Solvent Free ◽  
Coupling Reactions ◽  
Cross Coupling Reactions ◽  
Cross Coupling Reaction ◽  
Aqueous Conditions

An efficient solvent-free and aqueous protocol for the Buchwald–Hartwig cross-coupling reaction has been developed. Notably, the catalytic system also efficiently catalyzed the reaction under aqueous conditions.

Synthesis of a Cellulosic Pd(salen)-Type Catalytic Complex as a Green and Recyclable Catalyst for Cross-Coupling Reactions

2020 ◽  
Vol 150 (10) ◽  
pp. 2900-2910
Author(s):  
Peng Sun ◽  
Jiaojiao Yang ◽  
Chunxia Chen ◽  
Kaijun Xie ◽  
Jinsong Peng
Keyword(s):  
Cross Coupling ◽  
Recyclable Catalyst ◽  
Coupling Reactions ◽  
Catalytic Complex ◽  
Cross Coupling Reactions
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