Nickel(ii)-catalyzed direct arylation of aryl C–H bonds with aryl-boron reagents directed by a removable bidentate auxiliary
文献情報
Bin Liu, Zhuo-Zhuo Zhang, Xin Li, Bing-Feng Shi
Ni(II)-catalyzed C–H arylation using Ar2I+X− or ArX as the arylating reagent via oxidative addition has been well investigated. However, the analogous cross-coupling of C–H bonds with organoboron reagents via transmetallation remains a great challenge. Here we report the first Ni(II)-catalyzed direct C–H arylation with arylboronic acid esters assisted by a removable bidentate auxiliary. This procedure is scalable and compatible with a wide range of functional groups, providing a complementary protocol for the synthesis of biaryl compounds.
おすすめジャーナル

Acta Metallurgica Sinica-English Letters

Medicinal Chemistry Research

Bioorganic & Medicinal Chemistry

Cellulose

Herald of the Russian Academy of Sciences

Heteroatom Chemistry

Journal of Asian Natural Products Research

Biocatalysis and Biotransformation

Critical Reviews in Solid State and Materials Sciences

Polycyclic Aromatic Compounds
関連文献
Theoretical insights into unraveling the mechanism, selectivity patterns, and ligand effects in gold(i)-catalyzed annulations between ynamides and isoxazoles
Qing Sun, Jia-Jie Chen, Jia-Yi Liu, Wen-Qing Zhang, Xin Lu, Ren-Jie Song
DOI: 10.1039/D3QO01792C
Practical synthesis and divergent optimization of halichonine B for the discovery of novel pharmaceutical leads
Shengxin Sun, Juan Yang, Shengkun Li
DOI: 10.1039/D3QO01816D
Access to disulfides through ligand-controlled nickel-catalyzed dithiosulfonate and alkyl halides
Wang Chen, Xin-yu Liu, Yi-Fan Jiang, Weidong Rao, Shu-Su Shen, Zhao-Ying Yang, Shun-Yi Wang
DOI: 10.1039/D3QO01868G
Using pyrrolizine-fused bipolar PAHs as a new strategy towards efficient red and NIR emissive dyes
Krzysztof Bartkowski, Abhishek Kumar Gupta, Tomas Matulaitis, Maja Morawiak, Eli Zysman-Colman, Marcin Lindner
DOI: 10.1039/D3QO01914D
Pulsed electrolysis: enhancing primary benzylic C(sp3)–H nucleophilic fluorination
Alexander P. Atkins, Atul K. Chaturvedi, Joseph A. Tate, Alastair J. J. Lennox
DOI: 10.1039/D3QO01865B
Genome-driven discovery of new serrawettin W2 analogues from Serratia fonticola DSM 4576
Haolin Qiu, Yang Xiao, Ling Shen, Tao Han, Qiang He, Aiying Li, Peng Zhang
DOI: 10.1039/D3OB01642K
Enantio- and diastereoselective conjugate addition of pyridyl alkyl ketones to enones by Cu(ii)-Lewis acid/Brønsted base catalysis
Soojin Kwak, Minhyeok Lee, Eunji Sim, Sarah Yunmi Lee
DOI: 10.1039/D3QO01707A
Enantioselective synthesis of chiral BCPs
Irene Sánchez-Sordo, Sergio Barbeira-Arán, Martín Fañanás-Mastral
DOI: 10.1039/D3QO01631E
こちらもおすすめ
6-苄基-6,7-二氢-5H-吡咯并3,4-b吡啶とは何ですか?
6-苄基-6,7-二氢-5H-吡咯并3,4-b吡啶は、CAS番号109966-30-5の化合物です。これは、6-ベンジル基を持つ6,7-二氢-5H-吡咯並みの化...
半硫酸奎宁单水水合物はどのように保存すればよいですか?
半硫酸奎宁单水水合物は、乾燥した涼しい場所に保管し、直射日光や湿気を避ける必要があります。保存温度は常温(15〜25℃)が適切で、湿度は40%以下を維持すること...
D-核糖-5-リン酸二ナトリウムとは何ですか?
D-核糖-5-リン酸二ナトリウムは、CAS番号18265-46-8を有する化合物で、D-核糖の5位付加部位にリン酸基が結合した化合物です。この化合物は、水溶性で...
3-乙酰基-4-羟基喹啉-2(1H)-酮はどのように合成されますか?
3-乙酰基-4-羟基喹啉-2(1H)-酮は、ハイドロキノンと酢酸アセトイルアミドのアミド化反応により合成されます。この反応は塩基触媒を用いて行われ、選択性は良好...
5-溴-4-甲基-1H-吲唑とは何ですか?
5-溴-4-甲基-1H-吲唑は、CAS番号1082041-34-6の化学物質で、化学式はC10H9BrNです。この化合物は淡黄色の結晶性粉末で、吸湿性があります...
3-(4メトキシフェニル)オキテナン-3カーボイル酸の代替品はありますか?
3-(4メトキシフェニル)オキテナン-3カーボイル酸の代替品は、その用途により異なりますが、例えば4-(メトキシフェニル)オキテナン-3カーボイル酸や、他のオキ...
3-イリドオキシピロロ[2,3-b]ピリジン-5-カルボキシlic酸は安全ですか?
3-イリドオキシピロロ[2,3-b]ピリジン-5-カルボキシlic酸は危険な化合物ではありませんが、適切な手袋や保護眼鏡の使用を推奨します。誤って摂取または接触...
3-氟-4- iodobenolを取り扱う際の実験室安全事項は何ですか?
3-氟-4- iodobenolは可燃性を有し、強力な反応性を持つため、取り扱いには注意が必要です。PPE(個人保護具)の着用、ドラフトチャンバーの使用、漏洩時...
掲載誌
Organic Chemistry Frontiers

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry




