Cp*Co(iii) and Cu(OAc)2 bimetallic catalysis for Buchwald-type C–N cross coupling of aryl chlorides and amines under base, inert gas & solvent-free conditions

2020 ◽  
Vol 22 (23) ◽  
pp. 8248-8253
Author(s):  
Avinash K. Srivastava ◽  
Charu Sharma ◽  
Raj K. Joshi
Keyword(s):  
Cross Coupling ◽  
Solvent Free ◽  
Inert Gas ◽  
Coupling Reactions ◽  
Bimetallic Catalysis ◽  
Aryl Chlorides ◽  
Solvent Free Conditions ◽  
Type C

A strategy involving bimetallic catalysis which requires a combination of Cp*Co(CO)I2 and Cu(OAc)2 was used to perform Buchwald-type C–N coupling reactions of aryl chlorides with amines.

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The article has been withdrawn at the request of editor of the journal Current Organic Chemistry: Bentham Science apologizes to the readers of the journal for any inconvenience this may have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

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...

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.

Suzuki–Miyaura Cross‐Coupling under Solvent‐Free Conditions

2013 ◽  
Vol 355 (18) ◽  
pp. 3553-3557 ◽  
Author(s):  
Andrey F. Asachenko ◽  
Kristina R. Sorochkina ◽  
Pavel B. Dzhevakov ◽  
Maxim A. Topchiy ◽  
Mikhail S. Nechaev
Keyword(s):  
Cross Coupling ◽  
Solvent Free ◽  
Solvent Free Conditions
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