ChemInform Abstract: Recent Advances in Copper-Catalyzed Asymmetric Coupling Reactions

ChemInform ◽  
2016 ◽  
Vol 47 (12) ◽  
pp. no-no
Author(s):  
Fengtao Zhou ◽  
Qian Cai
Keyword(s):  
Coupling Reactions ◽  
Recent Advances ◽  
Asymmetric Coupling

Recent advances in transition-metal-catalysed asymmetric coupling reactions with light intervention

2021 ◽  
Author(s):  
Fu-Dong Lu ◽  
Jun Chen ◽  
Xuan Jiang ◽  
Jia-Rong Chen ◽  
Liang-Qiu Lu ◽  
...  
Keyword(s):  
Transition Metal ◽  
Coupling Reactions ◽  
Recent Advances ◽  
Modern Chemistry ◽  
Asymmetric Coupling

The advances on transition-metal catalysed asymmetric couplings with light intervention in recent years was summarized in this review. In order to better meet the needs of modern chemistry, further research outlook was also proposed.

scholarly journals Recent advances in copper-catalyzed asymmetric coupling reactions

2015 ◽  
Vol 11 ◽  
pp. 2600-2615 ◽  
Author(s):  
Fengtao Zhou ◽  
Qian Cai
Keyword(s):  
Recent Progress ◽  
Alkyl Halides ◽  
Coupling Reactions ◽  
Ring Systems ◽  
The Past ◽  
Recent Advances ◽  
Asymmetric Coupling ◽  
Significant Attention

Copper-catalyzed (or -mediated) asymmetric coupling reactions have received significant attention over the past few years. Especially the coupling reactions of aryl or alkyl halides with nucleophiles became a very powerful tool for the formation of C–C, C–N, C–O and other carbon–heteroatom bonds as well as for the construction of heteroatom-containing ring systems. This review summarizes the recent progress in copper-catalyzed asymmetric coupling reactions for the formation of C–C and carbon–heteroatom bonds.

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The article has been withdrawn at the request of editor of the journal Current Organic Chemistry: Bentham Science apologizes to the readers of the journal for any inconvenience this may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

scholarly journals Asymmetric Pd-NHC*-catalyzed coupling reactions

2012 ◽  
Vol 84 (8) ◽  
pp. 1741-1748 ◽  
Author(s):  
E. Peter Kündig ◽  
Yixia Jia ◽  
Dmitry Katayev ◽  
Masafumi Nakanishi
Keyword(s):  
High Temperature ◽  
Coupling Reactions ◽  
Structural Studies ◽  
Methylene Unit ◽  
Asymmetric Coupling ◽  
New Applications ◽  
Very High

Very high asymmetric inductions result in the Pd-catalyzed intramolecular arylation of amides to give 3,3-disubstituted oxindoles when new in situ-generated chiral N-heterocyclic carbene (NHC*) ligands are employed. Structural studies show that conformational locking to minimize allylic strain is the key to understanding the function of these ligands. New applications of these ligands in the frontier area of asymmetric coupling reactions involving C(sp3)–H bonds are detailed. Highly enantioenriched fused indolines are accessible using either preformed- or in situ-generated Pd-NHC* catalysts. Remarkably, this occurs at high temperature (140–160 °C) via excellent asymmetric recognition of an enantiotopic C–H bond in an unactivated methylene unit.

The recent advances in K2S2O8-mediated cyclization/coupling reactions via an oxidative transformation

2020 ◽  
Vol 56 (96) ◽  
pp. 15101-15117
Author(s):  
Sumit Kumar ◽  
Kishor Padala
Keyword(s):  
Organic Synthesis ◽  
Coupling Reactions ◽  
Oxidative Transformation ◽  
Recent Advances

Recently the K2S2O8 mediated cyclization/coupling reactions to construct carbon–carbon/carbon–heteroatom bond via oxidative transformation is became much interesting in organic synthesis.

Recent advances and perspectives in copper-catalyzed Sonogashira coupling reactions

RSC Advances ◽  
2014 ◽  
Vol 4 (42) ◽  
pp. 21688-21698 ◽  
Author(s):  
Anns Maria Thomas ◽  
Asha Sujatha ◽  
Gopinathan Anilkumar
Keyword(s):  
Coupling Reactions ◽  
Sonogashira Coupling ◽  
Recent Advances

The review highlights the origin, development, mechanistic insights and recent applications of Cu-catalyzed Sonogashira coupling reactions.

Recent Advances in Pd/C-Catalyzed Coupling Reactions

Synthesis ◽  
2006 ◽  
Vol 2006 (18) ◽  
pp. 2975-2992 ◽  
Author(s):  
Masahiko Seki
Keyword(s):  
Coupling Reactions ◽  
Recent Advances
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