The hamburger-shape photocatalyst: thioxanthone-based chiral [2.2]paracyclophane for enantioselective visible-light photocatalysis of 3-methylquinoxalin-2(1H)-one and styrenes
文献情報
Shou-Chih Huo, Ranadheer Reddy Indurmuddam, Bor-Cherng Hong, Chuan-Fu Lu, Su-Ying Chien
A new thioxanthone-based photocatalyst with a [2.2]paracyclophane skeleton and planar chirality has been developed. The catalyst has been successfully applied in the visible light-mediated enantioselective aza Paternò–Büchi reactions of quinoxalinone and styrenes to produce azetidines. The structures of the catalyst derivatives were unequivocally determined by their single crystal X-ray crystallography analysis.
おすすめジャーナル

Journal of the Indian Institute of Science

Acta Metallurgica Sinica-English Letters

Atomization and Sprays

NDT & E International

Medicinal Chemistry Research

Critical Reviews in Solid State and Materials Sciences

Herald of the Russian Academy of Sciences

Bioorganic & Medicinal Chemistry

Journal of Chemical Sciences

Electroanalysis
関連文献
New routes to manganese higher-nuclearity topologies: synthesis of the cluster [Mn8(μ4-O)4(phpz)8(thf)4]
Stefania Tanase, Guillem Aromí, Elisabeth Bouwman, Huub Kooijman, Anthony L. Spek, Jan Reedijk
DOI: 10.1039/B504215A
First osmium-catalysed ketamination of alkenes
Amparo Villar, Claas H. Hövelmann, Martin Nieger, Kilian Muñiz
DOI: 10.1039/B505278P
Enantioselective hydrogenation of alkenes and imines by a gold catalyst
Avelino Corma, Marta Iglesias, Felix Sánchez
DOI: 10.1039/B505271H
Halogen: A high-capacity cathode for rechargeable alkaline batteries
Jun-qing Pan, Yan-zhi Sun, Ping-yu Wan, Zi-hao Wang, Xiao-guang Liu
DOI: 10.1039/B504476F
Ionic diamine rhodium(i) complexes—highly active catalysts for the hydroformylation of olefins
Jai Jun Kim, Howard Alper
DOI: 10.1039/B502435H
The Hildebrand solubility parameters, cohesive energy densities and internal energies of 1-alkyl-3-methylimidazolium-based room temperature ionic liquids
Sang Hyun Lee, Sun Bok Lee
DOI: 10.1039/B503740A
Discrete dispersion of single-walled carbon nanotubes
Qingwen Li, Ian A. Kinloch, Alan H. Windle
DOI: 10.1039/B419039D
The influence of sterics on the formation of polar 1-D hydrogen-bonded networks
Adam J. Preston, Judith C. Gallucci, Jon R. Parquette
DOI: 10.1039/B414470H
Porous materials show superhydrophobic to superhydrophilic switching
Neil J. Shirtcliffe, Glen McHale, Michael I. Newton, Carole C. Perry, Paul Roach
DOI: 10.1039/B502896E
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 & Biomolecular Chemistry

Organic & Biomolecular Chemistry (OBC) publishes original and high impact research and reviews in organic chemistry. We welcome research that shows new or significantly improved protocols or methodologies in total synthesis, synthetic methodology or physical and theoretical organic chemistry as well as research that shows a significant advance in the organic chemistry or molecular design aspects of chemical biology, catalysis, supramolecular and macromolecular chemistry, theoretical chemistry, mechanism-oriented physical organic chemistry, medicinal chemistry or natural products. Articles published in the journal should report new work which makes a highly-significant impact in the field. Routine and incremental work is generally not suitable for publication in the journal. More details about key areas of our scope are below. In all cases authors should include in their article clear rationale for why their research has been carried out.
![1H-Imidazo[4,5-c]pyridine-7-carboxylic acid structure 1H-Imidazo[4,5-c]pyridine-7-carboxylic acid structure](https://static.chemtradehub.com/structs/123/1234616-39-7-1344.webp)

![5-Bromo-3-isopropyl-1H-pyrrolo[2,3-b]pyridine structure 5-Bromo-3-isopropyl-1H-pyrrolo[2,3-b]pyridine structure](https://static.chemtradehub.com/structs/125/1256819-54-1-8620.webp)
![(1R,6R)-6-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-cyclohexene-1-carboxylic acid structure (1R,6R)-6-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-cyclohexene-1-carboxylic acid structure](https://static.chemtradehub.com/structs/865/865689-24-3-5fef.webp)
