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Chemical Science, ISSN 2041-6520, 2018, Volume 9, Issue 33, pp. 6839 - 6843
Herein, we describe the first linear-selective hydroarylation reaction of unactivated alkenes and styrenes with aryl boronic acids, which was achieved by... 
H BOND ACTIVATION | OLEFIN HYDROARYLATION | DIRECTING GROUP | TRISUBSTITUTED ALKENES | BIOLOGICAL EVALUATION | CARBONYL-COMPOUNDS | CATALYTIC ASYMMETRIC HYDROBORATION | CHEMISTRY, MULTIDISCIPLINARY | C-H | ALIPHATIC ALKENES | VINYL ETHERS | Organic chemistry | Alkenes | Chemical synthesis | Styrenes | Aromatic compounds | Butyric acid
Journal Article
Journal of gastrointestinal surgery : official journal of the Society for Surgery of the Alimentary Tract, ISSN 1091-255X, 05/2019
Whether neoadjuvant chemotherapy (NAC) increased the risk of postoperative morbidities for patients with locally advanced gastric cancer (GC) is unknown.... 
Journal Article
ACS Catalysis, ISSN 2155-5435, 09/2016, Volume 6, Issue 9, pp. 5978 - 5988
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 12/2013, Volume 52, Issue 51, pp. 13676 - 13680
Colors to dye for: Palladium‐catalyzed regiospecific N‐heteroarylations of amidines with 2‐halo‐N‐heteroarenes leads to a structurally diverse library of... 
palladium | dyes and pigments | fluorescence | heterocycles | boron | HIGHLY FLUORESCENT | FLUOROPHORES | COVALENT BONDS | COMPLEXES | ARYLATION | CHEMISTRY, MULTIDISCIPLINARY | INTRAMOLECULAR CHARGE-TRANSFER | SOLID-STATE | BODIPY DYES | AGGREGATION-INDUCED EMISSION | DERIVATIVES | Fluorescence | Palladium | Green technology | Boron | Dyes | Luminescence | Fluid flow | Libraries | Difluorides
Journal Article
Organic Letters, ISSN 1523-7060, 09/2013, Volume 15, Issue 17, pp. 4504 - 4507
Herein, a rhodium(III)-catalyzed oxidative C–H activation of simple arylphosphonates and phosphonamides with subsequent coupling with alkenes (olefination),... 
H BOND ACTIVATION | OXIDATIVE OLEFINATION | ACID-DERIVATIVES | ARYLATION | ARENES | C-C | CHEMISTRY, ORGANIC | ARYL HYDROGEN PHOSPHATES | ALKYNES | CYCLIZATION | ALKENYLATION | Alkenes - chemistry | Cyclization | Oxidation-Reduction | Organophosphonates - chemistry | Alkynes - chemistry | Molecular Structure | Catalysis | Alkenes - chemical synthesis | Rhodium - chemistry
Journal Article
ISSN 2041-6520, 8/2018, Volume 9, Issue 33, pp. 6839 - 6843
Herein, we describe the first linear-selective hydroarylation reaction of unactivated alkenes and styrenes with aryl boronic acids, which was achieved by... 
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 05/2011, Volume 50, Issue 23, pp. 5365 - 5369
Journal Article
NATURE COMMUNICATIONS, ISSN 2041-1723, 11/2019, Volume 10, Issue 1, pp. 5025 - 10
The conventional oxidative Heck reaction between aryl boronic acids and alkenes typically involved the Pd-II/Pd-0/Pd-II catalytic cycle incorporating an... 
FUNCTIONALIZATION | HALIDES | ALKENES | HYDROCARBONS | MULTIDISCIPLINARY SCIENCES | BONDS | OLEFINS | HYDROARYLATION | CYCLIZATION | C-H | CARBOXYLIC-ACIDS | Alkenes | Regioselectivity | Catalysts | Aromatic compounds | Phosphine | Isomerization | Nickel | Selectivity | Hydrogenation | Optimization
Journal Article
Chemical Communications, ISSN 1359-7345, 08/2011, Volume 47, Issue 32, pp. 9188 - 9190
A new, efficient protocol for the synthesis of di(hetero)aryl sulfides is described. Cheap and easily available arylsulfonyl chlorides as a sulfur source... 
Sulfinic Acids - chemistry | Sulfides - chemical synthesis | Hydrocarbons, Aromatic - chemical synthesis | Sulfinic Acids - chemical synthesis | HALIDES | C-H BOND | 3-SULFENYL | COUPLINGS | CATALYZED SULFENYLATION | CHEMISTRY, MULTIDISCIPLINARY | INDOLES | SULFONYL CHLORIDES | DISULFIDES
Journal Article
by Walters, Raymond K and Polimanti, Renato and Johnson, Emma C and McClintick, Jeanette N and Adams, Mark J and Adkins, Amy E and Aliev, Fazil and Bacanu, Silviu Alin and Batzler, Anthony and Bertelsen, Sarah and Biernacka, Joanna M and Bigdeli, Tim B and Chen, Li Shiun and Clarke, Toni Kim and Chou, Yi Ling and Degenhardt, Franziska and Docherty, Anna R and Edwards, Alexis C and Fontanillas, Pierre and Foo, Jerome C and Fox, Louis and Frank, Josef and Giegling, Ina and Gordon, Scott and Hack, Laura M and Hartmann, Annette M and Hartz, Sarah M and Heilmann-Heimbach, Stefanie and Herms, Stefan and Hodgkinson, Colin and Hoffmann, Per and Jan Hottenga, Jouke and Kennedy, Martin A and Alanne-Kinnunen, Mervi and Konte, Bettina and Lahti, Jari and Lahti-Pulkkinen, Marius and Lai, Dongbing and Ligthart, Lannie and Loukola, Anu and Maher, Brion S and Mbarek, Hamdi and McIntosh, Anew M and McQueen, Matthew B and Meyers, Jacquelyn L and Milaneschi, Yuri and Palviainen, Teemu and Pearson, John F and Peterson, Roseann E and Ripatti, Samuli and Ryu, Euijung and Saccone, Nancy L and Salvatore, Jessica E and Sanchez-Roige, Sana and Schwandt, Melanie and Sherva, Richard and Streit, Fabian and Strohmaier, Jana and Thomas, Nathaniel and Wang, Jen Chyong and Webb, Bradley T and Wedow, Robbee and Wetherill, Leah and Wills, Amanda G and Agee, Michelle and Alipanahi, Babak and Auton, Adam and Bell, Robert K and Bryc, Katarzyna and Elson, Sarah L and Furlotte, Nicholas A and Hinds, David A and Huber, Karen E and Kleinman, Aaron and Litterman, Nadia K and McCreight, Jennifer C and McIntyre, Matthew H and Mountain, Joanna L and Noblin, Elizabeth S and Northover, Carrie A.M and Pitts, Steven J and Sathirapongsasuti, J. Fah and Sazonova, Olga V and Shelton, Janie F and Shringarpure, Suyash and Tian, Chao and Tung, Joyce Y and Vacic, Vladimir and Wilson, Catherine H and Boardman, Jason D and Chen, Danfeng and Choi, Doo Sup and Copeland, William E and Culverhouse, Robert C and Dahmen, Norbert and Degenhardt, Louisa and Domingue, Benjamin W and Frye, Mark A and Gäbel, Wolfgang and Hayward, Caroline and ... and 23Andme Res Team and 23andMe Research Team
Nature Neuroscience, ISSN 1097-6256, 11/2018, Volume 21, Issue 12, pp. 1656 - 1669
Journal Article