Article
Chemistry, Multidisciplinary
Qiaoli Li, Lanting Xu, Dawei Ma
Summary: Direct N-arylation of sulfonamides using a combination of copper and oxalamides (or 4-hydroxypicolinamides) as catalysts is an efficient method. It allows for a wide range of reactions between sulfonamides and (hetero)aryl bromides, and even works well with primary sulfonamides and (hetero)aryl chlorides under the catalysis of Cu2O and a 4-hydroxypicolinamide.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
(2022)
Article
Chemistry, Physical
Xufeng Ma, Han Wang, Yao Liu, Xing Zhao, Jun Zhang
Summary: Mixed alkyl/aryl diphos ligands have shown enhanced activity and selectivity in iron-catalyzed cross coupling reactions, with the electronic effect of the ligands playing a crucial role in catalytic performance. Fe catalyst supported by L8 exhibited the best catalytic performance and good functional group tolerance.
Article
Chemistry, Physical
Xiaojun Zeng, Chao Wang, Wenhao Yan, Jian Rong, Yanshan Song, Zhiwei Xiao, Aijie Cai, Steven H. Liang, Wei Liu
Summary: Despite the historical challenge of engaging unactivated alkyl halides in Sonogashira coupling reactions, we have developed a strategy that combines Cu-catalyzed alkyne transfer with aryl radical activation of carbon-halide bonds. This allows for a general approach to coupling alkyl iodides with terminal alkynes. This unprecedented reaction tolerates a wide range of functional groups and has been applied to the late-stage cross-coupling of pharmaceutical agents and the synthesis of positron emission tomography tracers.
Article
Chemistry, Multidisciplinary
Aijie Cai, Wenhao Yan, Chao Wang, Wei Liu
Summary: In this study, a novel strategy was developed to utilize the halogen abstraction ability of aryl radicals in copper-catalyzed Negishi-type cross-coupling reactions, allowing a diverse range of alkyl iodides to participate at room temperature.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
(2021)
Article
Chemistry, Physical
Xiaojun Zeng, Chao Wang, Wenhao Yan, Jian Rong, Yanshan Song, Zhiwei Xiao, Aijie Cai, Steven H. Liang, Wei Liu
Summary: A new strategy combining Cu-catalyzed alkyne transfer with aryl radical activation of carbon-halide bonds enables the coupling of alkyl iodides with terminal alkynes. This unprecedented Sonogashira-type cross coupling reaction is tolerant towards a wide range of functional groups and has applications in pharmaceutical synthesis and the synthesis of positron emission tomography tracers.
Article
Chemistry, Multidisciplinary
Qingmin Man, Zunyun Fu, Tiantian Liu, Mingyue Zheng, Hualiang Jiang
Summary: The mechanism of Cu catalyzed intramolecular Ullmann C=O coupling reaction was investigated using density functional theory, revealing a four-step reaction process involving oxidative addition, coordination effect, ligand exchange, and reductive elimination. The results were in good agreement with experimental data, providing insights into the Ullmann reaction mechanism.
ACTA CHIMICA SINICA
(2021)
Article
Chemistry, Physical
Fengqian Zhao, Patrizio Russo, Raffaella Mancuso, Bartolo Gabriele, Xiao-Feng Wu
Summary: A copper-catalyzed carbonylation of alkyl iodides with phenols is reported, yielding corresponding esters in good yields. Aliphatic alcohols are also suitable partners in this reaction.
JOURNAL OF CATALYSIS
(2022)
Article
Chemistry, Multidisciplinary
Yujiro Hayashi, Shusuke Hattori, Seitaro Koshino
Summary: Flow reactions using an immobilized diphenylprolinol alkyl ether catalyst 2 were investigated for alpha,beta-unsaturated aldehydes and nitroalkanes. The reactions showed fast reaction rates and excellent enantioselectivity with good overall yields and turnover numbers.
CHEMISTRY-AN ASIAN JOURNAL
(2022)
Review
Chemistry, Multidisciplinary
Meng-Yu Xu, Bin Xiao
Summary: Palladium-catalyzed cross-coupling reactions play a crucial role in the complex synthetic field. Our research group focuses on developing new germanium-based reagents and catalytic processes. Over the past three years, we have established new methods for the synthesis of novel compounds, with particular emphasis on the unique properties of alkyl carbagermatranes.
CHEMICAL COMMUNICATIONS
(2021)
Article
Multidisciplinary Sciences
Connor P. Delaney, Eva Lin, Qinan Huang, Isaac F. Yu, Guodong Rao, Lizhi Tao, Ana Jed, Serena M. Fantasia, Kurt A. Puentener, R. David Britt, John F. Hartwig
Summary: Copper complexes catalyze cross-coupling reactions through a newly discovered mechanism. The copper(II) complexes catalyze Ullmann coupling by synthesizing the C-O bond through concerted oxidative addition. This mechanism allows for high turnover numbers and the reactions can be performed in air.
Article
Chemistry, Physical
Xiaodong Ma, Guozhu Zhang
Summary: This study describes a copper-catalyzed, highly enantioselective alkyl and aryl/azolation of alkenes, where the use of a specific chiral ligand plays a crucial role in the success of the chemistry. Anionic tridentate ligands are employed to enhance the reducibility of copper complexes, facilitating the generation of alkyl/aryl radicals and providing good enantiocontrol in the azolation. The three-component coupling reactions have mild reaction conditions and can tolerate a broad range of functional groups, allowing for the straightforward introduction of valuable azole functionalities into complex molecular systems through direct C-H functionalization.
Article
Chemistry, Organic
Giorgio Rizzo, Gianluigi Albano, Teresa Sibillano, Cinzia Giannini, Roberta Musio, Fiorenzo G. Omenetto, Gianluca M. Farinola
Summary: This paper reports the application of a silk fibroin-supported Palladium catalyst (Pd/SF) in Suzuki-Miyaura and Ullmann coupling reactions of aryl chlorides. The existence of catalytic pockets where monoatomic palladium species can form stable complexes with SF is hypothesized and supported by experimental analysis. The size of the catalytic pocket of Pd/SF is estimated to be approximately 15 angstroms using computational modeling.
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
(2022)
Article
Chemistry, Multidisciplinary
Ying Chen, Lanting Xu, Yongwen Jiang, Dawei Ma
Summary: The combination of copper salts and oxalic diamides enables the synthesis of α-(hetero)aryl nitriles via one-pot decarboxylation under mild conditions. The method demonstrates a broad substrate scope and compatibility with various functionalities and heteroaryls.
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
(2021)
Article
Chemistry, Organic
Baiyao Zhu, Wenfang Xiong, Xiaobin Tan, Wanqing Wu, Huanfeng Jiang
Summary: A copper-catalyzed Ullmann-type C-N cross-coupling reaction of carbazole with aryl chlorides has been developed using N,N'-bis(thiophene-2-ylmethyl)oxalamide as ligand, which efficiently affords N-arylcarbazole.
TETRAHEDRON LETTERS
(2022)
Article
Chemistry, Multidisciplinary
Mingming Huang, Man Tang, Jiefeng Hu, Stephen A. Westcott, Udo Radius, Todd B. Marder
Summary: A Cu-catalysed borylation reaction can achieve high-yield synthesis of arylboronic esters from aryl alkyl sulfones, while selective cleavage of cyclic sulfones can be achieved through Cu-mediated or Cu-free processes to prepare sulfonyl-containing boronate esters.
CHEMICAL COMMUNICATIONS
(2022)
Article
Chemistry, Applied
Surya Srinivas Kotha, Nidhi Sharma, Govindasamy Sekar
ADVANCED SYNTHESIS & CATALYSIS
(2016)
Article
Chemistry, Applied
Dhanarajan Arunprasath, Govindasamy Sekar
ADVANCED SYNTHESIS & CATALYSIS
(2017)
Article
Chemistry, Applied
Nidhi Sharma, Govindasamy Sekar
ADVANCED SYNTHESIS & CATALYSIS
(2016)
Article
Chemistry, Organic
Govindharaj Kumar, Alagesan Muthukumar, Govindasamy Sekar
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
(2017)
Article
Chemistry, Organic
Somraj Guha, Imran Kazi, Anuradha Nandy, Govindasamy Sekar
EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
(2017)
Article
Chemistry, Organic
Sindhura Badigenchala, Govindasamy Sekar
JOURNAL OF ORGANIC CHEMISTRY
(2017)
Article
Chemistry, Organic
Pandi Muthupandi, Nallappan Sundaravelu, Govindasamy Sekar
JOURNAL OF ORGANIC CHEMISTRY
(2017)
Article
Chemistry, Organic
Alagesan Muthukumar, Govindasamy Sekar
ORGANIC & BIOMOLECULAR CHEMISTRY
(2017)
Article
Chemistry, Organic
Imran Kazi, Somraj Guha, Govindasamy Sekar
Article
Chemistry, Organic
Subramani Sangeetha, Govindasamy Sekar
Article
Chemistry, Organic
Dhanarajan Arunprasath, Balasubramanian Devi Bala, Govindasamy Sekar
Article
Chemistry, Organic
Selvaraj Chandrasekar, Iyyanar Karthikeyan, Govindasamy Sekar
SYNTHESIS-STUTTGART
(2018)
Article
Chemistry, Applied
Naziya Parveen, Rajib Saha, Govindasamy Sekar
ADVANCED SYNTHESIS & CATALYSIS
(2017)
Article
Chemistry, Multidisciplinary
Somraj Guha, Imran Kazi, Pranamita Mukherjee, Govindasamy Sekar
CHEMICAL COMMUNICATIONS
(2017)
Article
Chemistry, Applied
Nidhi Sharma, Rajib Saha, Naziya Parveen, Govindasamy Sekar
ADVANCED SYNTHESIS & CATALYSIS
(2017)
Article
Chemistry, Organic
Geeta Devi Yadav, Pooja Chaudhary, Balaram Pani, Surendra Singh
Summary: Chiral transition metal complexes with privileged ligands are efficient catalysts for various asymmetric organic transformations. Transition metal complexes of C1-symmetric pyrrolidine-based ligands have been widely used in asymmetric organic reactions. However, a comprehensive review article on the transition metal complexes of chiral C1-symmetric pyrrolidine-based ligands derived from (L)-proline has not been published.
TETRAHEDRON LETTERS
(2024)