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Journal of the American Chemical Society, ISSN 0002-7863, 09/2016, Volume 138, Issue 35, pp. 11132 - 11135
Cross-couplings of alkyl halides and organometallic species based on single electron transfer using Ni and Fe catalyst systems have been studied extensively,... 
ARYL GRIGNARD-REAGENTS | CUBANES | KUMADA | REACTIVITY | CHEMISTRY | IRON | ELECTRON-TRANSFER MECHANISM | BETA-HYDROGENS | SECONDARY ALKYL-HALIDES | CHEMISTRY, MULTIDISCIPLINARY | Oxidation-reduction reaction | Usage | Iron compounds | Chemical properties | Catalysts | Carbon compounds | Index Medicus | Communication
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2016, Volume 55, Issue 33, pp. 9676 - 9679
A transformation analogous in simplicity and functional group tolerance to the venerable Suzuki cross‐coupling between alkyl‐carboxylic acids and boronic acids... 
decarboxylation | redox-active esters | homogeneous catalysis | nickel catalysts | Suzuki cross-coupling | HALIDES | ARYLATIONS | PHOTOREDOX | BROMIDES | CHEMISTRY, MULTIDISCIPLINARY | IODIDES | ALKYL ELECTROPHILES | ELECTRON-TRANSFER MECHANISM | Nickel | Catalysis | Organic compounds | Acids | Cross coupling | Transformation | Esters | Carboxylic acids | Functional groups | Index Medicus
Journal Article
Synthesis (Germany), ISSN 0039-7881, 2015, Volume 47, Issue 1, pp. 134 - 140
An efficient and practical method was developed for the synthesis of 2,2-disubstituted indolin-3-ones by palladium-catalyzed asymmetric allylic alkylation.... 
indolines | palladium | allylic substitution | asymmetric catalysis | quaternary carbon | CARBON CENTERS | ALLYLATION | CHEMISTRY, ORGANIC | ENANTIOSELECTIVE CONSTRUCTION | AMINATION | AMINO-ACIDS | BIOSYNTHESIS | DIELS-ALDER REACTION | 1ST TOTAL-SYNTHESIS | REGIO | DUOCARMYCIN
Journal Article
Synthesis, ISSN 0039-7881, 01/2015, Volume 47, Issue 1, pp. 134 - 140
Abstract An efficient and practical method was developed for the synthesis of 2,2-disubstituted indolin-3-ones by palladium-catalyzed asymmetric allylic... 
paper
Journal Article
Angewandte Chemie (International ed. in English), ISSN 1433-7851, 8/2016, Volume 55, Issue 33, pp. 9676 - 9679
A transformation analogous in simplicity and functional group tolerance to the venerable Suzuki cross-coupling between alkyl-carboxylic acids and boronic acids... 
decarboxylation | esters | redox-active | Suzuki | nickel catalysis
Journal Article
Nature, ISSN 0028-0836, 08/2018, Volume 560, Issue 7718, pp. 350 - 354
Prized for their ability to rapidly generate chemical complexity by building new ring systems and stereocentres(1), cycloaddition reactions have featured in... 
POTENT | REDOX-ACTIVE ESTERS | MULTIDISCIPLINARY SCIENCES | EPOTHILONES | Ring formation (Chemistry) | Research | Drug discovery | Carbon-carbon composites | Cross coupling | Chemical reactions | Hybridization | Enantiomers | Kinases | Modularity | Carbon | Complexity | Organic chemistry | Chemistry | Cycloaddition | Teaching methods | Natural products | Chemical synthesis | Coupling methods | Index Medicus
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2019, Volume 58, Issue 8, pp. 2454 - 2458
Journal Article
Chemical Communications, ISSN 1359-7345, 06/2014, Volume 50, Issue 51, pp. 6751 - 6753
Journal Article
中国物理B:英文版, ISSN 1674-1056, 2015, Volume 24, Issue 1, pp. 315 - 320
An all-fiber optical modulator, which is composed of a piece of no-core fiber spliced between two sections of singlemode fibers and uses magnetic fluid(MF) as... 
全光纤 | 磁流体 | 磁场强度 | 磁性流体 | 单模光纤 | 光调制器 | No-core fiber | Magnetic fluid | Optical modulator | Optical fiber | magnetic fluid | optical fiber | no-core fiber | optical modulator | ABSORPTION | PHYSICS, MULTIDISCIPLINARY | Optical fibers | Dynamic response | Wavelengths | Magnetic fields | Cladding | Magnetic fluids | Optimization | Modulators
Journal Article
Angewandte Chemie, ISSN 0044-8249, 02/2019, Volume 131, Issue 8, pp. 2476 - 2480
This work bridges a gap in the cross‐coupling of aliphatic redox‐active esters with aryl zinc reagents. Previously limited to primary, secondary, and... 
Nickel-Katalyse | Decarboxylierende Radikalkupplungen | Tertiäre Säuren | Quartäre Zentren | Redoxaktive Ester | Esters | Nickel | Catalysis | Chemical tests and reagents | Organic acids | Aromatic compounds | Quaternary | Reagents | Carboxylic acids | Coupling | Zinc | Aliphatic compounds
Journal Article
Guangdianzi Jiguang/Journal of Optoelectronics Laser, ISSN 1005-0086, 03/2013, Volume 24, Issue 3, pp. 558 - 562
Journal Article
Angewandte Chemie, ISSN 0044-8249, 08/2016, Volume 128, Issue 33, pp. 9828 - 9831
A transformation analogous in simplicity and functional group tolerance to the venerable Suzuki cross‐coupling between alkyl‐carboxylic acids and boronic acids... 
Homogene Katalyse | Decarboxylierung | Nickel-Katalysatoren | Redoxaktive Ester | Suzuki-Kreuzkupplung | Nickel | Organic compounds | Cross coupling | Esters | Activation | Transformations | Tolerances | Derivatives | Carboxylic acids
Journal Article
Angewandte Chemie, ISSN 0044-8249, 08/2016, Volume 128, Issue 33, p. 9828
  A transformation analogous in simplicity and functional group tolerance to the venerable Suzuki cross-coupling between alkyl-carboxylic acids and boronic... 
Acids | Cross coupling | Transformation | Esters | Nickel | Carboxylic acids | Functional groups
Journal Article
Guangdianzi Jiguang/Journal of Optoelectronics Laser, ISSN 1005-0086, 02/2015, Volume 26, Issue 2, pp. 288 - 294
Journal Article
Guangdianzi Jiguang/Journal of Optoelectronics Laser, ISSN 1005-0086, 02/2013, Volume 24, Issue 2, pp. 302 - 307
Journal Article
Guangdianzi Jiguang/Journal of Optoelectronics Laser, ISSN 1005-0086, 11/2014, Volume 25, Issue 11, pp. 2136 - 2140
Journal Article
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