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Chemical Society reviews, ISSN 1460-4744, 2016, Volume 45, Issue 23, pp. 6462 - 6477
..., 45,6 4 6 2 of C–H activation and ring scission Fen Wang, Songjie Yu and Xingwei Li* Organic transformations that involve direct functionalization of C–H bonds... 
HETEROBICYCLIC ALKENES | FUNCTIONALIZATION | ACTIVATION/CYCLOADDITION | PYRIDOTRIAZOLES | HETEROCYCLES | S-ARYL SULFOXIMINES | METHYLENECYCLOPROPANES | AMIDATION | BOND-CLEAVAGE | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | Couplings | Transition metals | Aromatic compounds | Chemical bonds | Strategy | Activation | Transformations | Scission
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2016, Volume 55, Issue 30, pp. 8696 - 8700
Previous direct C−H nitrogenation suffered from simple amidation/amination with limited atom‐economy and is mostly limited to C(sp2)−H substrates. In this... 
reaction mechanisms | amination | C−H activation | arenes | rhodium | ROOM-TEMPERATURE | ACTIVATION | INTRAMOLECULAR C(SP)-H | AZIDES | INTERMOLECULAR AMIDATION | ALKYNES | CHEMISTRY, MULTIDISCIPLINARY | C-H activation | COUPLING REACTIONS | CARBON-NITROGEN BONDS | C-H AMINATION | Catalysis
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2016, Volume 55, Issue 49, pp. 15351 - 15355
Functionalizable directing groups (DGs) are highly desirable in C−H activation chemistry. The nitrone DGs are explored in rhodium(III)‐catalyzed C−H activation... 
small ring compounds | reaction mechanisms | C−H activation | arenes | rhodium | ROOM-TEMPERATURE | OXYGEN-ATOM TRANSFER | INTERNAL ALKYNES | BOND-CLEAVAGE | CHEMISTRY, MULTIDISCIPLINARY | CATALYZED ANNULATIONS | FUNCTIONALIZATION | QUINOLINE N-OXIDES | C-H activation | CYCLIZATION | CARBOXYLIC-ACIDS | RHODIUM CATALYSIS | Rhodium
Journal Article
Chemical science (Cambridge), ISSN 2041-6539, 2018, Volume 9, Issue 4, pp. 973 - 978
The first transition metal-catalyzed stereoconvergent Markovnikov 1,2-hydrosilylation of ( / )-dienes was effectively achieved with excellent -selectivities... 
PLATINUM-CARBENE COMPLEXES | ASYMMETRIC HYDROSILYLATION | ACTIVATION | 1,3-DIENES | HOMOGENEOUS CATALYSIS | TERMINAL ALKYNES | REGIO | STEREOSELECTIVE HYDROSILYLATION | CHEMISTRY, MULTIDISCIPLINARY | ALKENE HYDROSILYLATION | TERTIARY SILANES | Catalysts | Regioselectivity | Aromatic compounds | Isomerization | Hydrosilylation | Catalysis | Dienes | Cobalt
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2017, Volume 56, Issue 50, pp. 15896 - 15900
An asymmetric copper‐catalyzed alkylation of quinoline N‐oxides with chiral Cu–alkyl species, generated by migratory insertion of a vinylarene into a chiral... 
quinoline N-oxides | alkylation | copper | vinylarenes | asymmetric catalysis | ASYMMETRIC-SYNTHESIS | REAGENTS | ALPHA-ARYLATION | PYRIDINES | CHEMISTRY, MULTIDISCIPLINARY | UNACTIVATED ALKENES | FORMAL HYDROAMINATION | H BOND ADDITION | CROSS-COUPLING REACTIONS | ARYL HALIDES | CUH | Quinoline | Alkaloids | Oxides | Catalysis | Enantiomers | Copper | Quinolines | Migratory species | N-Oxides | Alkylation | Organic compounds
Journal Article
ISSN 2041-6520, 1/2018, Volume 9, Issue 4, pp. 973 - 978
...Chemical Science EDGE ARTICLE Cobalt-catalyzed regioselective stereoconvergent Markovnikov 1,2-hydrosilylation of conjugated dienes† Hui Leng Sang, Songjie Yu... 
Journal Article
Organic Letters, ISSN 1523-7060, 01/2015, Volume 17, Issue 1, pp. 58 - 61
Journal Article
Cell research, ISSN 1748-7838, 2018, Volume 28, Issue 8, pp. 855 - 861
...ARTICLE BE-PLUS: a new base editing tool with broadened editing window and enhanced fidelity Wen Jiang1, Songjie Feng2,3,4, Shisheng Huang2, Wenxia Yu2... 
SYSTEM | HUMAN EMBRYOS | PROTEIN | DEAMINASE FUSIONS | TARGET BASE | DNA | MUTATIONS | HYPERMUTATION | MAMMALIAN-CELLS | GENOME | CELL BIOLOGY | Word processing | Fidelity | Software reviews | Gene disruption | Editing | Genomes | Codons | Cytidine deaminase
Journal Article
Organic Letters, ISSN 1523-7060, 07/2013, Volume 15, Issue 14, pp. 3706 - 3709
Rhodium(III)-catalyzed C–H activation–amidation of arenes bearing chelating groups has been achieved using N-arenesulfonated imides as efficient amidating... 
ALKENES | ELECTRON | MECHANISM | VERSATILE | CHLOROAMINES | REACTIVITY | CHEMISTRY, ORGANIC | BOND FORMATION | CATALYZED DIRECT AMINATION | ISOCYANATES | ALKYNES | Imides - chemistry | Hydrogen Bonding | Sulfhydryl Compounds - chemistry | Molecular Structure | Catalysis | Indicators and Reagents - chemistry | Rhodium - chemistry
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 05/2017, Volume 359, Issue 10, pp. 1620 - 1625
An efficient synthesis of 2‐substituted quinolines from readily available cyclopropanols and imidamides has been developed, where the cyclopropanol acts as a... 
imidamides | C–H activation | 2-substituted quinolines | cyclopropanols | C–N bond formation | C-N bond formation | RING EXPANSION | ONE-POT SYNTHESIS | ANNULATION | CHEMISTRY, ORGANIC | INTERNAL ALKYNES | OXIME ESTERS | FUNCTIONALIZATION | C-H activation | HETEROCYCLES | N BOND FORMATION | METAL | ARYL | CHEMISTRY, APPLIED | Carbon-carbon composites | Cleavage | Rhodium | Chemical synthesis | Organic compounds
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 2013, Volume 52, Issue 9, pp. 2577 - 2580
Making CC from CH: [{RhCp*Cl2}2]/AgSbF6 (Cp*=pentamethylcyclopentadienyl) can regioselectively catalyze the CC coupling of arenes with aziridines by a CH... 
aziridines | CH activation | CC coupling | rhodium | C-C coupling | C-H activation | DIRECTING GROUP | ARYLATION | OXIDATIVE ANNULATION | ALKYNES | CHEMISTRY, MULTIDISCIPLINARY | CC coupling | FUNCTIONALIZATION | EFFICIENT CATALYST | CH activation | VERSATILE | N BOND FORMATION | ARYL | ELECTRON-RICH ARENES | Insertion | Activation | Joining | Pathways | Aromatic compounds | Bonding
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 05/2017, Volume 359, Issue 10, pp. 1599 - 1599
The front cover picture, provided by Xingwei Li and co‐workers, illustrates an efficient synthesis of 2‐substituted quinolines from readily available... 
imidamides | C–H activation | 2-substituted quinolines | cyclopropanols | C–N bond formation | Carbon-carbon composites | Cleavage | Rhodium | Chemical synthesis | Organic compounds
Journal Article
IOP Conference Series: Earth and Environmental Science, ISSN 1755-1307, 10/2018, Volume 186, Issue 2
Conference Proceeding