Correction: Transition metal-catalyzed direct remote C–H functionalization of alkyl groups via C(sp3)–H bond activation
文献情報
Guanyinsheng Qiu
Correction for ‘Transition metal-catalyzed direct remote C–H functionalization of alkyl groups via C(sp3)–H bond activation’ by Guanyinsheng Qiu, et al., Org. Chem. Front., 2015, 2, 169–178.
おすすめジャーナル

Electroanalysis

Polycyclic Aromatic Compounds

Critical Reviews in Solid State and Materials Sciences

Medicinal Chemistry Research

Biocatalysis and Biotransformation

Chinese Journal of Chemistry

Bioorganic & Medicinal Chemistry

Acta Metallurgica Sinica-English Letters

Atomization and Sprays

Journal of Chemical Sciences
関連文献
Carbon atom insertion into N-heterocyclic carbenes to yield 3,4-dihydroquinoxalin-2(1H)-ones
Justin S. Lamb, Futa Koyama, Noriyuki Suzuki, Yumiko Suzuki
DOI: 10.1039/D3QO01579C
Asymmetric permanganate dihydroxylation of enoates: substrate scope, mechanistic insights and application in bicalutamide synthesis
Peilong Gu, Shuangshuang Wang, Xiangxiang Wen, Jinxin Tian, Chao Wang, Lili Zong, Choon-Hong Tan
DOI: 10.1039/D3QO01729J
Correction: An efficient metal free synthesis of 2-aminobenzothiozoles – a greener approach
Ganesh Sambasivam, Govindarajulu Gavara, Ramraj S, Gaikwad Rajendra, Karthikeyan Sivashanmugam
DOI: 10.1039/D3OB90143B
Serine-mediated hydrazone ligation displaying insulin-like peptides on M13 phage pIII
Nan Zheng, Danny Hung-Chieh Chou
DOI: 10.1039/D3OB01487H
Halogen bonding and mechanochemistry combined: synthesis, characterization, and application of N-iodosaccharin pyridine complexes
Khai-Nghi Truong, Jas S. Ward, Rakesh Puttreddy, Anssi Rajala, Elias Lassila, Carsten Bolm, Kari Rissanen
DOI: 10.1039/D3QO01512B
Photoredox Ni-catalyzed decarboxylative arylation of oxamic acids for amide synthesis
Depeng Duan, Lu Song
DOI: 10.1039/D3QO01370G
Copper-catalyzed crosscoupling of vinyl nitrenes and CF3-carbenes to synthesize CF3-2-azadienes
Yongjuan Jiao, Tao Wu, Xinyu Zhang
DOI: 10.1039/D3QO01537H
A route to carbon-sp3 bridging spiro-molecules: synthetic methods and optoelectronic applications
DOI: 10.1039/D3QO01735D
N-Sulfenyl phthalimide enabled Markovnikov hydrothiolation of unactivated alkenes via ligand promoted cobalt catalysis
Xiang-Rui Li, Rong-Jin Zhang, Yonghong Xiao, Qing-Xiao Tong
DOI: 10.1039/D3QO01632C
A de novo synthesis of the bisindole alkaloid geissolosimine: collective synthesis of geissoschizoline, akuammicine, (16S)-deshydroxymethylstemmadenine and Aspidospermatan alkaloids
Jiahang Yan, Yanxia Zhen, Pengyan Wang, Yimeng Han, Huanhuan Zou, Junhan Chen, Weigang He
DOI: 10.1039/D3QO01898A
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


![2-Methyl-2-propanyl {3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-3-oxetanyl}carbamate structure 2-Methyl-2-propanyl {3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-3-oxetanyl}carbamate structure](https://static.chemtradehub.com/structs/127/1279090-25-3-1b84.webp)
![[5-fluoro-2-(morpholine-4-carbonyl)phenyl]boronic acid structure [5-fluoro-2-(morpholine-4-carbonyl)phenyl]boronic acid structure](https://static.chemtradehub.com/structs/121/1217501-26-2-505c.webp)
