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Angewandte Chemie International Edition, ISSN 1433-7851, 11/2017, Volume 56, Issue 48, pp. 15441 - 15445
The use of transition‐metal catalysis to enable the coupling of readily available organic molecules has greatly enhanced the ability of chemists to access... 
cross-coupling | nickel | ketones | Heck reactions | acylation | CARBENE | HYDROGENATION | COMPLEXES | BOND FORMATION | PALLADIUM CATALYSIS | AROMATIC-ALDEHYDES | CHEMISTRY, MULTIDISCIPLINARY | DIRECT ACYLATION | DERIVATIVES | ARYL CHLORIDES | Ketones | Aldehydes | Chemical reactions | Coupling (molecular) | Organic chemistry | Transformation | Chemists | Nickel | Selectivity | Catalysis | Friedel-Crafts reaction | Carbonyls
Journal Article
Synlett, ISSN 0936-5214, 10/2018, Volume 29, Issue 16, pp. 2081 - 2086
Abstract The classical Heck reaction is among the most powerful methods available for the construction of C–C bonds. Modification of this transformation to... 
synpacts | cross-coupling | Heck reaction | nickel | high-throughput experimentation | reaction discovery | C-H BOND | DIARYL KETONES | CHEMISTRY, ORGANIC | AROMATIC-ALDEHYDES | SINGLE-ELECTRON TRANSMETALATION | ARYLBORONIC ACIDS | DIRECT ACYLATION | PHOTOREDOX CATALYSIS | ARYL HALIDES | COUPLING REACTION | ASYMMETRIC ALKENE HYDROGENATION
Journal Article
ACS Catalysis, ISSN 2155-5435, 03/2017, Volume 7, Issue 3, pp. 2176 - 2180
A palladium-catalyzed cross-coupling between aryl esters and anilines is reported, enabling access to diverse amides. The reaction takes place via activation... 
cross-coupling | palladium catalysis | amides | C-N coupling | C-O bond activation | CATALYZED DECARBONYLATIVE BORYLATION | ORGANOBORON COMPOUNDS | C-O ACTIVATION | NICKEL CATALYSIS | cross-coupling amides | ARYL ESTERS | CHEMISTRY, PHYSICAL | ARYLBORONIC ACIDS | PHENOL DERIVATIVES | BORONIC ACIDS | KETONE SYNTHESIS | ATMOSPHERIC-PRESSURE
Journal Article
Organic Letters, ISSN 1523-7060, 07/2018, Volume 20, Issue 13, pp. 4094 - 4098
The Pd-catalyzed cross-coupling of phenyl esters and alkyl boranes is disclosed. Two reaction modes are rendered accessible in a selective fashion by... 
ORGANOBORON COMPOUNDS | BORONIC ACIDS | O BOND ACTIVATION | C-O | KETONE SYNTHESIS | NICKEL CATALYSIS | ARYL ESTERS | NHC PRECATALYST | CHEMISTRY, ORGANIC | SUZUKI-MIYAURA | ARYLBORONIC ACIDS
Journal Article
Organic Letters, ISSN 1523-7060, 03/2015, Volume 17, Issue 6, pp. 1521 - 1524
I2–TBHP-catalyzed oxidative cross coupling of N-sulfonyl hydrazones with isocyanides has been realized for the synthesis of 5-aminopyrazoles through formal [4... 
Journal Article
Synlett, ISSN 0936-5214, 12/2017, Volume 28, Issue 20, pp. 2851 - 2854
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 02/2015, Volume 21, Issue 8, pp. 3193 - 3197
A simple and straightforward approach was developed to construct 5H‐benzo[b]carbazole derivatives by iron catalysis in a cascade sequence. The notable features... 
iron | sulfonyl migration | benzo[b]carbazoles | pericyclic reaction | alkynes | Benzo[b]carbazoles | Iron | Pericyclic reaction | Sulfonyl migration | Alkynes | CARBAZOLES | CHEMISTRY, MULTIDISCIPLINARY | CYCLOADDITION | YNAMIDES | ETHERS | FACILE | DERIVATIVES | CYCLIZATION | Catalysis | Carbazoles | Migration | Chemical synthesis | Carbazole | Functional groups | Economics | Cascades | Tolerances | Derivatives
Journal Article
Bioorganic & Medicinal Chemistry, ISSN 0968-0896, 2009, Volume 17, Issue 13, pp. 4681 - 4692
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 05/2015, Volume 2015, Issue 14, p. 3171
A facile and efficient Ag.sub.I-catalytic approach is reported for the first time to synthesize [beta]-oxo amides from [beta]-oxo esters a with broad substrate... 
Amides | Esters
Journal Article
Synlett, ISSN 0936-5214, 12/2017, Volume 28, Issue 20, pp. 2851 - 2854
Abstract A procedure is presented that enables the direct deuteration of the formyl C–H bond of aldehydes using D 2 O as the deuterium source and commercially... 
letter | deuteration | COMPLEXES | H | CHEMISTRY, ORGANIC | DEUTERIUM | ALCOHOLS | REARRANGEMENT | ruthenium | aldehydes | isotopic labeling | RADIOLABELED COMPOUNDS | D exchange | CYCLIZATION | AMIDES
Journal Article
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 05/2016, Volume 2016, Issue 13, pp. 2284 - 2289
A sequential one‐pot approach towards arylated benzoquinones and naphthoquinones is reported. The reaction proceeds through oxidation of phenols/naphthols... 
Quinones | Triflic acid | Cytotoxicity | Synthetic methods | Metal‐free | Metal-free | ARYLQUINONES | CHEMISTRY, ORGANIC | SYSTEMS | C-H FUNCTIONALIZATION | AROMATIC-COMPOUNDS | DERIVATIVES | CONJUGATE ADDITION
Journal Article
Synthetic Communications, ISSN 0039-7911, 10/2016, Volume 46, Issue 19, pp. 1612 - 1618
A new one-pot synthetic methodology has been developed to construct the triazole-linked urea derivatives. In the same step, triazole forms from azide and... 
triazoles | copper catalysis | one-pot reaction | BCC cell lines | urea | AZIDE-ALKYNE CYCLOADDITION | CHEMISTRY, ORGANIC | MULTICOMPONENT | CARBONYLATION | AMINES | 1,2,3-TRIAZOLES | BIOLOGY | REGIOSELECTIVE SYNTHESIS | CHEMISTRY | INHIBITORS
Journal Article
Chemical Communications, ISSN 1359-7345, 06/2014, Volume 50, Issue 51, pp. 6726 - 6728
A practical one-pot hypoiodite catalysed oxidative cyclization approach to synthesize alpha-ketobenzoxazole derivatives was successfully developed. This... 
KETONES | INHIBITORS | ACID AMIDE HYDROLASE | CHEMISTRY, MULTIDISCIPLINARY | METAL-FREE | CYCLIZATION | Ethers - chemical synthesis | Oxidants - chemistry | Cyclization | Iodine Compounds - chemistry | Oxidation-Reduction | Indicators and Reagents | Catalysis | Benzoxazoles - chemical synthesis
Journal Article
Chemical Communications: Chem Comm, ISSN 1359-7345, 05/2014, Volume 50, Issue 51, pp. 6726 - 6728
A practical one-pot hypoiodite catalysed oxidative cyclization approach to synthesize alpha -ketobenzoxazole derivatives was successfully developed. This... 
Synthesis (chemistry) | Substrates | Derivatives
Journal Article
Organic Letters, ISSN 1523-7060, 09/2012, Volume 14, Issue 17, pp. 4478 - 4481
An expedient method for a direct approach to the selective and regiocontrolled synthesis of 2-oxazolines and 2-oxazoles mediated by ZnI2 and FeCl3 is... 
GOLD CATALYSIS | PROPARGYLAMIDES | COMPLEXES | CHEMISTRY, ORGANIC | EFFICIENT | STRAIGHTFORWARD SYNTHESIS | CYCLIZATION | Lewis Acids - chemistry | Zinc Compounds - chemistry | Oxazoles - chemical synthesis | Cyclization | Ferric Compounds - chemistry | Iodides - chemistry | Molecular Structure | Catalysis | Chlorides - chemistry | Oxazoles - chemistry
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 10/2014, Volume 2014, Issue 28, pp. 6219 - 6226
A highly regioselective and efficient base‐catalyzed intramolecular hydroalkoxylation of primary and secondary alkynyl alcohols was developed to afford... 
Synthetic methods | Nitrogen heterocycles | Cyclization | Regioselectivity | Hydroamination | Alkynes | MODE CYCLIZATION | CHEMISTRY, ORGANIC | BRANCHING CASCADE | OXYGEN | HYDROALKOXYLATION | CATALYTIC ASYMMETRIC-SYNTHESIS | ACCESS | Chemotherapy | Cancer
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 09/2015, Volume 357, Issue 13, pp. 2788 - 2794
A mild and efficient transition metal‐free approach has been developed for the synthesis of highly substituted chiral morpholines from alkenols by amino... 
halo‐etherification | λ3‐iodanes | morpholines | 6‐exo‐trig cyclization | alkenes
Journal Article
Tetrahedron, ISSN 0040-4020, 2011, Volume 67, Issue 46, pp. 8895 - 8901
A novel way of synthesizing unsymmetrical disulfides from thiols with DDQ is presented here. This procedure ran in a straightforward manner to give high... 
DDQ | Thiol | Oxidation | Symmetrical and unsymmetrical | Disulfide | DESIGN | PROTEIN | ONE-POT SYNTHESIS | CHEMISTRY, ORGANIC | BOND FORMATION | THIOLS | GLYCOSYL DISULFIDES | ORGANIC DISULFIDES | DIARYL DISULFIDES | 1-CHLOROBENZOTRIAZOLE | Thiols | Tetrahedrons | Synthesis (chemistry) | Disulfides
Journal Article
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, ISSN 0002-7863, 05/2019, Volume 141, Issue 17, pp. 6869 - 6874
An intermolecular coupling of primary alcohols and organotriflates has been developed to provide ketones by the action of a Ni(0) catalyst. This oxidative... 
SECONDARY ALCOHOLS | TRANSFORMATION | ACTIVATION | OPPENAUER OXIDATION | CONVERSION | BORROWING HYDROGEN | CARBONYL ADDITION | ALLYLATION | ARYL | ALDEHYDES | CHEMISTRY, MULTIDISCIPLINARY
Journal Article
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