Pd(ii)-catalyzed intermolecular enantioselective hydroamination of styrenes
Literature Information
Feng Yu, Pinhong Chen, Guosheng Liu
A Pd-catalyzed intermolecular asymmetric hydroamination of styrenes was developed to give various chiral benzyl amides exclusively, in which the oxidation-stable pyridine-oxazoline was used as the chiral ligand to provide moderate to good enantioselectivities.
Related Literature
A novel three-component coupling reaction of aryne, CN derivatives, and acrylonitrile
Yangang Wu, Wenbo Cai, Lulu Yu, Junbiao Chang, Chuanjun Song
DOI: 10.1039/D3QO01454A
Isatin-based spiro indolenine alkaloids from Isatis indigotica Fortune with anti-neuroinflammatory and acetylcholinesterase inhibitory effects
Ming Bai, Yu-Fei Xi, Si-Hui Mi, Pei-Yuan Yang, Li-Li Lou, Tian-Ming Lv, Xin Zhang, Guo-Dong Yao, Bin Lin, Shao-Jiang Song
DOI: 10.1039/D3QO01769A
Azaborahelicene fluorophores derived from four-coordinate N,C-boron chelates: synthesis, photophysical and chiroptical properties
José Francisco Rizo, Jesús F. Arteaga, Ludovic Favereau, Abel Ros, Uwe Pischel
DOI: 10.1039/D3QO01762A
Pd-catalyzed vinyl C–H amination with diaziridinone
Jianjun Wang, Huiying Hong, Daguo Hu, Jieling Liu, Wei Liu, Yian Shi
DOI: 10.1039/D3QO01472J
Photoredox Suzuki coupling using alkyl boronic acids and esters
Kanak Kanti Das, Somenath Mahato, Debraj Ghorai, Sutapa Dey, Santanu Panda
DOI: 10.1039/D3QO01838E
A deconstruction–reconstruction strategy to access 1-naphthol derivatives: application to the synthesis of aristolactam scaffolds
Jeong Min Bak, Moonyeong Song, Inji Shin, Hee Nam Lim
DOI: 10.1039/D3OB01603J
Advances in photoinduced radical–polar crossover cyclization (RPCC) of bifunctional alkenes
Meng Liu, Xinke Ouyang, Chenglong Xuan
DOI: 10.1039/D3QO01929B
Photoredox catalyzed release of carbon-based radicals from 2-substituted-1,3-imidazolidines
Adrián Luguera Ruiz, Elena Mariani, Stefano Protti, Maurizio Fagnoni
DOI: 10.1039/D3QO01856C
Diastereoselective 1,2-difunctionalization of 1,3-enynes enabled by merging photoexcited Hantzsch ester with chromium catalysis
Jia Wu, Xiangyun Xu, Chongwen Duan, Shan Chen, Dan Wang, Likui Fang, Weiyang Tang, Fusheng Li
DOI: 10.1039/D3QO01522J
Atroposelective synthesis of N–N axially chiral pyrrolyl(aza)-quinolinone by de novo ring formation
Qiwen Huang, Yanze Li, Cun Yang, Wendan Wu, Jingjie Hai, Xinyao Li
DOI: 10.1039/D3QO01877F
You might also like
How should 2-Methylbenzene-1,4-diamine dihydrochloride (CAS: 615-45-2) be stored?
2-Methylbenzene-1,4-diamine dihydrochloride (CAS: 615-45-2) should be stored in ...
Is (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide (CAS: 132747-20-7) safe?
(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide is generally considered sa...
What industries use (6-Chloropyridazin-3-YL)methanamine (CAS: 871826-15-2)?
(6-Chloropyridazin-3-YL)methanamine finds applications in the pharmaceutical ind...
What are the main uses of 2-Fluoro-3-methylphenol (CAS: 77772-72-6)?
2-Fluoro-3-methylphenol is primarily used in the synthesis of pharmaceuticals, p...
What precautions should be taken when handling 3-Methoxy-4-nitrobenzonitrile (CAS: 177476-75-4)?
When handling 3-Methoxy-4-nitrobenzonitrile, it is important to wear appropriate...
What precautions should be taken when handling 1,3-Oxazolo[4,5-b]pyridine-2(3H)-thione (CAS: 211949-57-4)?
When handling 1,3-Oxazolo[4,5-b]pyridine-2(3H)-thione (CAS: 211949-57-4), it is ...
What regulatory guidelines apply to 4-Ethynylbenzamide (CAS: 90347-86-7)?
4-Ethynylbenzamide (CAS: 90347-86-7) falls under various regulatory guidelines i...
What are the main uses of 3-(2-Ethylphenyl)-2-thioxo-4-imidazolidinone (CAS: 186822-57-1)?
3-(2-Ethylphenyl)-2-thioxo-4-imidazolidinone is primarily used as an intermediat...
What is (2-Fluoro-6-methoxyphenyl)acetic acid (CAS: 500912-19-6)?
(2-Fluoro-6-methoxyphenyl)acetic acid, also known as 4-fluoro-3-methoxybenzoic a...
What is the market or research trend for 2-[4-(Hydroxymethyl)phenoxy]ethanol (CAS: 102196-18-9)?
Market trends for 2-[4-(Hydroxymethyl)phenoxy]ethanol (CAS: 102196-18-9) indicat...
Source Journal
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














