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Angewandte Chemie International Edition, ISSN 1433-7851, 04/2013, Volume 52, Issue 18, pp. 4929 - 4932
New S in town: Sulfonyl hydrazides smoothly undergo sulfenylation with indoles in the presence of 10 mol % I2 to give structurally diverse indole thioethers in... 
regioselectivity | hydrazides | iodine | heterocycles | synthetic methods | REAGENTS | 3-SULFENYLATION | ARYLATION | TOSYLHYDRAZONES | CHEMISTRY, MULTIDISCIPLINARY | CHLORIDES | INHIBITORS | EFFICIENT SULFENYLATION | Hydrazines - chemistry | Iodine - chemistry | Oxidation-Reduction | Stereoisomerism | Catalysis | Indoles - chemistry | Sulfur - chemistry | Towns | Synthesis | Indoles | Hydrazides | Sulfur
Journal Article
Chemical Communications, ISSN 1359-7345, 03/2015, Volume 51, Issue 21, pp. 4433 - 4436
A new nanocluster of atomic precision, Au44(SC2H4Ph)32, is obtained by an oxidation–decomposition–recombination (ODR) process from Au25(SC2H4Ph)18 under mild... 
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 10/2017, Volume 56, Issue 41, pp. 12644 - 12648
Although face‐centered cubic (fcc), body‐centered cubic (bcc), hexagonal close‐packed (hcp), and other structured gold nanoclusters have been reported, it was... 
gold | electrochemical gap | differential pulse voltammetry | nanoclusters | structure elucidation | X-ray crystallography | Kernels | Gold | Single crystals | Packing | Electrochemistry | Close packed lattices | Crystallography | Crystal structure
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2012, Volume 51, Issue 12, pp. 2968 - 2971
The NH2 group serves as an effective leaving group in the palladium‐catalyzed regioselective and stereospecific title reaction (see scheme). The reaction works... 
palladium | cross‐coupling | boron | CN bond cleavage | allylic compounds | cross-coupling | C-N bond cleavage | C?N bond cleavage | CARBON-NITROGEN | ALKYLATION | N-BENZYLIC SULFONAMIDES | CHEMISTRY, MULTIDISCIPLINARY | SUZUKI-MIYAURA | ALLYLAMINES | ALCOHOLS | NUCLEOPHILES | REARRANGEMENT | ACETATES | DERIVATIVES
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 04/2018, Volume 360, Issue 7, pp. 1544 - 1548
A tandem radical carbamoylation/cyclization reaction of N‐arylacrylamides with hydrazinecarboxamides has been developed for facile access to... 
oxindoles | carbamoylation | cyclization | acrylamides | hydrazinecarboxamides | 3,3-DISUBSTITUTED OXINDOLES | ALKOXYCARBONYLATION | CHEMISTRY, ORGANIC | METAL-FREE SYNTHESIS | DIFUNCTIONALIZATION | ACTIVATED ALKENES | ARYL ACRYLAMIDES | SULFONYL HYDRAZIDES | OLEFINS | RADICALS | CHEMISTRY, APPLIED | BOND | Copper compounds | Copper | Carbonates | Butyl hydroperoxide
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 04/2019, Volume 25, Issue 20, pp. 5169 - 5172
A new strategy has been established for the synthesis of polysubstituted morpholin‐2‐ones through Stevens rearrangements of tertiary amines via in situ... 
amines | ammonium ylides | morpholin-2-ones | epoxides | Stevens rearrangement | Chemical industry | Ammonium | Amines | Synthesis | Regioselectivity | Catalysts | Acids | Quaternary | Amino acids | Epoxides | Zinc | Intermediates
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2014, Volume 53, Issue 14, pp. 3684 - 3687
A highly efficient strategy for the kinetic resolution of axially chiral BINAM derivatives involving a chiral Brønsted acid‐catalyzed imine formation and... 
axial chirality | enantioselectivity | kinetic resolution | Brønsted acids | BINAM | MANNICH | TRANSFER HYDROGENATION | THIOUREA ORGANOCATALYST | HANTZSCH ESTERS | CHEMISTRY, MULTIDISCIPLINARY | CYCLOADDITION | CROSS-COUPLING REACTIONS | RELAY CATALYSIS | REDUCTION | PHOSPHORIC-ACID | Bronsted acids | ALPHA-IMINO ESTERS
Journal Article
中国化学:英文版, ISSN 1001-604X, 2017, Volume 35, Issue 5, pp. 567 - 571
Tuning the nanoclusters' compositions and structures is critical for the performance improvement of nanoclusters.Herein,a well-known Au25(SCH2CH2Ph)18 (Au25... 
doping | catalysis | peeling | gold nanocluster | A3‐coupling reaction | coupling reaction | Catalysis | Peeling | Doping | Gold nanocluster
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 02/2013, Volume 355, Issue 2‐3, pp. 337 - 340
A highly regioselective halogenation reaction of symmetrical and unsymmetrical aromatic azo compounds has been developed at room temperature or at 50 °C. In... 
regioselectivity | palladium | iodination | aromatic azo compounds | bromination | Iodination | Aromatic azo compounds | Palladium | Regioselectivity | Bromination | REAGENTS | CARBON | COMPLEXES | ARYLATION | REACTIVITY | CHEMISTRY, ORGANIC | C-H BONDS | FUNCTIONALIZATION | SELECTIVE ORTHO-BROMINATION | AMINES | ANILINES | CHEMISTRY, APPLIED | Aromatic compounds
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 03/2015, Volume 357, Issue 5, pp. 928 - 932
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 09/2012, Volume 134, Issue 36, pp. 14694 - 14697
Journal Article
Chemical Communications, ISSN 1359-7345, 05/2012, Volume 48, Issue 40, pp. 4899 - 4901
A range of 3H-indoles and 2H-benzo[b][1,4]thiazines smoothly undergo asymmetric Strecker reaction with ethyl cyanoformate in the presence of a Cinchona... 
ASYMMETRIC CATALYSIS | CYANATION | KETIMINES | ET2ALCN | CHEMISTRY, MULTIDISCIPLINARY | IMINES | Formates - chemistry | Stereoisomerism | Imines - chemistry | Cinchona - chemistry | Catalysis | Thiourea - chemistry | Thiazines - chemistry | Cinchona Alkaloids - chemistry | Asymmetry | Catalysts | Thioureas
Journal Article