Chemical Reviews, ISSN 0009-2665, 10/2017, Volume 117, Issue 19, p. 12281
Advances in the chemical synthesis of C-pyranosides/furanosides are summarized, covering the literature from 2000 to 2016. The majority of the methods take...
Carbon-carbon composites | Phosphates | Linkages | Construction | Glycosylation | Carbon | Acetates | Lactones | Stereoselectivity | Molecules | Halides | Chemical bonds | Chemical synthesis | Coordination compounds | Metal complexes | Sugars | Sulfones
Carbon-carbon composites | Phosphates | Linkages | Construction | Glycosylation | Carbon | Acetates | Lactones | Stereoselectivity | Molecules | Halides | Chemical bonds | Chemical synthesis | Coordination compounds | Metal complexes | Sugars | Sulfones
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 2017, Volume 15, Issue 9, pp. 1947 - 1955
The synthesis of sulfones via a selective functionalization of C-H-bonds represents a powerful alternative to classical methods for the preparation of this...
Sulfones - chemistry | Molecular Structure | Sulfones - chemical synthesis
Sulfones - chemistry | Molecular Structure | Sulfones - chemical synthesis
Journal Article
Chemical Reviews, ISSN 0009-2665, 06/2010, Volume 110, Issue 6, pp. 3600 - 3740
CONCISE ASYMMETRIC-SYNTHESIS | HUMAN MELANOCORTIN-4 RECEPTOR | TRIFLUOROMETHYLATED ALLYLIC AMINES | UNSATURATED 1,2-AMINO ALCOHOLS | ALPHA-AMINO-ACIDS | DIFLUOROMETHYL PHENYL SULFONE | HIGHLY STEREOSELECTIVE-SYNTHESIS | RHODIUM-CATALYZED ADDITION | CHEMISTRY, MULTIDISCIPLINARY | N-SULFINYL IMINES | POTENT FUNCTIONAL AGONISTS | Amines - chemistry | Oxidation-Reduction | Sulfonamides - chemistry | Amino Alcohols - chemical synthesis | Stereoisomerism | Butanes - chemical synthesis | Amino Acids - chemistry | Amines - chemical synthesis | Amino Acids - chemical synthesis | Sulfonamides - chemical synthesis | Imines - chemistry | Diamines - chemistry | Organometallic Compounds - chemistry | Butanes - chemistry | Catalysis | Imines - chemical synthesis | Amino Alcohols - chemistry | Aziridines - chemistry | Diamines - chemical synthesis | Aziridines - chemical synthesis | Amines | Chemical properties | Tertiary butyl compounds | Structure | Chemical synthesis | Analysis
Journal Article
ORGANIC PROCESS RESEARCH & DEVELOPMENT, ISSN 1083-6160, 09/2007, Volume 11, Issue 5, pp. 913 - 917
A practical synthesis of 2-benzenesulfonylpyridine, 1, is described which is a key starting material for the manufacture of an investigational new drug...
OXIDATION | SULFOXIDES | THIOLS | ACID | S BOND | SULFIDES | CHEMISTRY, ORGANIC | HYDROGEN-PEROXIDE | SULFONES | CHEMISTRY, APPLIED | EFFICIENT | CATALYSTS
OXIDATION | SULFOXIDES | THIOLS | ACID | S BOND | SULFIDES | CHEMISTRY, ORGANIC | HYDROGEN-PEROXIDE | SULFONES | CHEMISTRY, APPLIED | EFFICIENT | CATALYSTS
Journal Article
Chemistry - A European Journal, ISSN 0947-6539, 09/2017, Volume 23, Issue 49, p. 11977
We developed a widely applicable, highly efficient synthesis of [alpha]-fluorosulfone and [beta]-fluorovinylsulfone catalyzed by gold. Starting with alkynyl...
Chemical synthesis | Gold | Vinyl sulfone
Chemical synthesis | Gold | Vinyl sulfone
Journal Article
Organic Letters, ISSN 1523-7060, 11/2010, Volume 12, Issue 21, pp. 4952 - 4955
An efficient room-temperature method for the synthesis of 1-sulfonyl-1,2,3-triazoles from in situ generated copper(I) acetylides and sulfonyl azides is...
ROOM-TEMPERATURE | CYCLOADDITION | SULFONYL AZIDES | REACTIVITY | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | COPPER | REARRANGEMENTS | WATER | Ligands | Triazoles - chemical synthesis | Molecular Structure | Copper - chemistry | Sulfones - chemistry
ROOM-TEMPERATURE | CYCLOADDITION | SULFONYL AZIDES | REACTIVITY | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | COPPER | REARRANGEMENTS | WATER | Ligands | Triazoles - chemical synthesis | Molecular Structure | Copper - chemistry | Sulfones - chemistry
Journal Article
Chemical Reviews, ISSN 0009-2665, 01/2015, Volume 115, Issue 2, pp. 765 - 825
ALPHA,BETA-UNSATURATED CARBOXYLIC-ACIDS | COPPER-CATALYZED TRIFLUOROMETHYLATION | TRIMETHYLSILYL FLUOROSULFONYLDIFLUOROACETATE TFDA | ONE-POT SYNTHESIS | PD(II)-CATALYZED ORTHO-TRIFLUOROMETHYLATION | MEDIATED REDUCTIVE TRIFLUOROMETHYLATION | DIFLUOROMETHYL PHENYL SULFONE | HIGHLY STEREOSELECTIVE-SYNTHESIS | CHEMISTRY, MULTIDISCIPLINARY | C-H BONDS | PENTAFLUOROSULFANYL SF5 SUBSTITUENTS | Sulfur compounds | Chemical properties | Chemical synthesis | Fluorine | Analysis | Electric properties
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 03/2018, Volume 360, Issue 6, pp. 1303 - 1303
Journal Article
Mini-Reviews in Organic Chemistry, ISSN 1570-193X, 2010, Volume 7, Issue 4, pp. 272 - 281
Given the pharmacological importance of resveratrol, preparation methods, including plant extraction, chemical synthesis and biotechnological production are...
Biotechnological production | Plant extraction | Bioavailability | Chemical synthesis | Structure-activity relationship | Resveratrol | plant extraction | ESCHERICHIA-COLI | SYNTHASE GENE-EXPRESSION | STILBENE SYNTHASE | CHEMISTRY, ORGANIC | CANCER CHEMOPREVENTIVE AGENT | CELL-CULTURES | chemical synthesis | PERFORMANCE LIQUID-CHROMATOGRAPHY | IN-VITRO | bioavailability | biotechnological production | TRANS-RESVERATROL | VITIS-VINIFERA | structure-activity relationship | 3,5-BIS(TRIFLUOROMETHYL)PHENYL SULFONES
Biotechnological production | Plant extraction | Bioavailability | Chemical synthesis | Structure-activity relationship | Resveratrol | plant extraction | ESCHERICHIA-COLI | SYNTHASE GENE-EXPRESSION | STILBENE SYNTHASE | CHEMISTRY, ORGANIC | CANCER CHEMOPREVENTIVE AGENT | CELL-CULTURES | chemical synthesis | PERFORMANCE LIQUID-CHROMATOGRAPHY | IN-VITRO | bioavailability | biotechnological production | TRANS-RESVERATROL | VITIS-VINIFERA | structure-activity relationship | 3,5-BIS(TRIFLUOROMETHYL)PHENYL SULFONES
Journal Article
Organic Letters, ISSN 1523-7060, 02/2015, Volume 17, Issue 3, pp. 736 - 739
A one-pot three-component protocol for the preparation of arylsulfonyl alkynes through the reaction of ethynyl-benziodoxolone (EBX) reagents, DABSO...
ORGANIC-SYNTHESIS | HYPERVALENT IODINE | HETEROCYCLES | SULFUR-DIOXIDE | CATALYZED SYNTHESIS | CHEMISTRY | CHEMISTRY, ORGANIC | ALKYNYLATING REAGENTS | DIARYLIODONIUM SALTS | ALKYNYLIODONIUM SALTS | EBX | Alkynes - chemical synthesis | Sulfones - chemistry | Indicators and Reagents | Alkynes - chemistry | Molecular Structure | Catalysis | Palladium - chemistry | Sulfones - chemical synthesis | Letter
ORGANIC-SYNTHESIS | HYPERVALENT IODINE | HETEROCYCLES | SULFUR-DIOXIDE | CATALYZED SYNTHESIS | CHEMISTRY | CHEMISTRY, ORGANIC | ALKYNYLATING REAGENTS | DIARYLIODONIUM SALTS | ALKYNYLIODONIUM SALTS | EBX | Alkynes - chemical synthesis | Sulfones - chemistry | Indicators and Reagents | Alkynes - chemistry | Molecular Structure | Catalysis | Palladium - chemistry | Sulfones - chemical synthesis | Letter
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 09/2013, Volume 78, Issue 18, pp. 9499 - 9504
Halosulfonylation of terminal alkynes was achieved with sulfonylhydrazides as the sulfonyl precursor and inexpensive iron halide as halide source in the...
DIFUNCTIONALIZATION | BETA-CHLOROVINYL SULFONES | ACETYLENES | ALKENES | CROSS-COUPLING REACTIONS | HALOGEN-METAL EXCHANGE | VINYL SULFONES | CATALYZED ALLYLIC SULFONYLATION | CHLORIDES | CHEMISTRY, ORGANIC | DERIVATIVES | Hydrazines - chemistry | Vinyl Compounds - chemical synthesis | Vinyl Compounds - chemistry | Stereoisomerism | Sulfones - chemistry | Bromides - chemistry | Ferric Compounds - chemistry | Alkynes - chemistry | Molecular Structure | Chlorides - chemistry | Sulfones - chemical synthesis | Iron compounds | Chemical properties | Research
DIFUNCTIONALIZATION | BETA-CHLOROVINYL SULFONES | ACETYLENES | ALKENES | CROSS-COUPLING REACTIONS | HALOGEN-METAL EXCHANGE | VINYL SULFONES | CATALYZED ALLYLIC SULFONYLATION | CHLORIDES | CHEMISTRY, ORGANIC | DERIVATIVES | Hydrazines - chemistry | Vinyl Compounds - chemical synthesis | Vinyl Compounds - chemistry | Stereoisomerism | Sulfones - chemistry | Bromides - chemistry | Ferric Compounds - chemistry | Alkynes - chemistry | Molecular Structure | Chlorides - chemistry | Sulfones - chemical synthesis | Iron compounds | Chemical properties | Research
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 08/2011, Volume 50, Issue 34, pp. 7837 - 7841
Spiral bound: The Morita–Baylis–Hillman adducts were employed as C3 synthons in the asymmetric [3+2] annulation with malonitrile substrates using...
phosphines | asymmetric synthesis | cycloaddition | spiro compounds | amino acids | (-)-VERSICOLAMIDE B | VINYL SULFONE | FUNCTIONALIZED CYCLOPENTENES | SPIROCYCLIC OXINDOLES | CHEMISTRY, MULTIDISCIPLINARY | MODIFIED ALLYLIC COMPOUNDS | SELECTIVE MANNICH REACTIONS | CATALYTIC ASYMMETRIC-SYNTHESIS | PHOSPHORUS YLIDE REACTION | N-TOSYLIMINES | ELECTRON-DEFICIENT OLEFINS | Threonine - chemistry | Chemistry Techniques, Synthetic | Phosphines - chemistry | Cyclization | Stereoisomerism | Spiro Compounds - chemical synthesis | Indoles - chemical synthesis | Molecular Structure | Catalysis | Indoles - chemistry | Spiro Compounds - chemistry
phosphines | asymmetric synthesis | cycloaddition | spiro compounds | amino acids | (-)-VERSICOLAMIDE B | VINYL SULFONE | FUNCTIONALIZED CYCLOPENTENES | SPIROCYCLIC OXINDOLES | CHEMISTRY, MULTIDISCIPLINARY | MODIFIED ALLYLIC COMPOUNDS | SELECTIVE MANNICH REACTIONS | CATALYTIC ASYMMETRIC-SYNTHESIS | PHOSPHORUS YLIDE REACTION | N-TOSYLIMINES | ELECTRON-DEFICIENT OLEFINS | Threonine - chemistry | Chemistry Techniques, Synthetic | Phosphines - chemistry | Cyclization | Stereoisomerism | Spiro Compounds - chemical synthesis | Indoles - chemical synthesis | Molecular Structure | Catalysis | Indoles - chemistry | Spiro Compounds - chemistry
Journal Article
Journal of Medicinal Chemistry, ISSN 0022-2623, 07/2013, Volume 56, Issue 14, pp. 5675 - 5690
The synthesis, preclinical profile, and in vivo efficacy in rat xenograft models of the novel and selective anaplastic lymphoma kinase inhibitor 15b (LDK378)...
CELL LUNG-CANCER | CHEMISTRY, MEDICINAL | SOLID TUMORS | GENE | DRUG DISCOVERY | C-MET | NON-HODGKINS-LYMPHOMA | ANTITUMOR-ACTIVITY | IDENTIFICATION | RECEPTOR TYROSINE KINASE | EXPERIMENTAL-MODELS | Protein Kinase Inhibitors - pharmacokinetics | Protein Kinase Inhibitors - chemical synthesis | Sulfones - therapeutic use | Pyrimidines - chemical synthesis | Humans | Macaca fascicularis | Rats | Male | Structure-Activity Relationship | Sulfones - pharmacokinetics | Neoplasms - drug therapy | Xenograft Model Antitumor Assays | Animals | Protein Kinase Inhibitors - therapeutic use | Pyrimidines - therapeutic use | Dogs | Pyrimidines - pharmacokinetics | Receptor Protein-Tyrosine Kinases - antagonists & inhibitors | Clinical Trials, Phase I as Topic | Clinical Trials, Phase II as Topic | Sulfones - chemical synthesis
CELL LUNG-CANCER | CHEMISTRY, MEDICINAL | SOLID TUMORS | GENE | DRUG DISCOVERY | C-MET | NON-HODGKINS-LYMPHOMA | ANTITUMOR-ACTIVITY | IDENTIFICATION | RECEPTOR TYROSINE KINASE | EXPERIMENTAL-MODELS | Protein Kinase Inhibitors - pharmacokinetics | Protein Kinase Inhibitors - chemical synthesis | Sulfones - therapeutic use | Pyrimidines - chemical synthesis | Humans | Macaca fascicularis | Rats | Male | Structure-Activity Relationship | Sulfones - pharmacokinetics | Neoplasms - drug therapy | Xenograft Model Antitumor Assays | Animals | Protein Kinase Inhibitors - therapeutic use | Pyrimidines - therapeutic use | Dogs | Pyrimidines - pharmacokinetics | Receptor Protein-Tyrosine Kinases - antagonists & inhibitors | Clinical Trials, Phase I as Topic | Clinical Trials, Phase II as Topic | Sulfones - chemical synthesis
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 09/2013, Volume 135, Issue 37, pp. 13652 - 13655
A stereoselective method for synthesis of trans-2,3-disubstituted 2,3-dihydropyrroles is reported. N-Sulfonyl-1,2,3-triazoles prepared from terminal alkynes...
AZAVINYL CARBENES | DIHYDROPYRROLE | ENANTIOSELECTIVE SYNTHESIS | CATALYZED TRANSANNULATION | CONTROLLING SELECTIVITY | MANNICH CYCLIZATION | OLEFIN CYCLOPROPANATION | REARRANGEMENTS | DERIVATIVES | 1-SULFONYL-1,2,3-TRIAZOLES | CHEMISTRY, MULTIDISCIPLINARY | Stereoisomerism | Triazoles - chemistry | Alkynes - chemistry | Azides - chemistry | Pyrroles - chemical synthesis | Sulfones - chemistry | Pyrroles - chemistry | Triazoles - chemical synthesis | Molecular Structure | Catalysis | Rhodium - chemistry | Aldehydes - chemistry | Sulfones - chemical synthesis
AZAVINYL CARBENES | DIHYDROPYRROLE | ENANTIOSELECTIVE SYNTHESIS | CATALYZED TRANSANNULATION | CONTROLLING SELECTIVITY | MANNICH CYCLIZATION | OLEFIN CYCLOPROPANATION | REARRANGEMENTS | DERIVATIVES | 1-SULFONYL-1,2,3-TRIAZOLES | CHEMISTRY, MULTIDISCIPLINARY | Stereoisomerism | Triazoles - chemistry | Alkynes - chemistry | Azides - chemistry | Pyrroles - chemical synthesis | Sulfones - chemistry | Pyrroles - chemistry | Triazoles - chemical synthesis | Molecular Structure | Catalysis | Rhodium - chemistry | Aldehydes - chemistry | Sulfones - chemical synthesis
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 01/2016, Volume 55, Issue 2, pp. 747 - 750
A redox‐neutral palladium(II)‐catalyzed conversion of aryl, heteroaryl, and alkenyl boronic acids into sulfinate intermediates, and onwards to sulfones and...
oxidation | palladium | sulfur | synthetic methods | electrophiles | SULFONE SYNTHESIS | ONE-POT | DIARYLIODONIUM SALTS | SULFONAMIDES | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | ALKYL-HALIDES | ARYL HALIDES | SULFUR-DIOXIDE SURROGATE | PALLADIUM-CATALYZED AMINOSULFONYLATION | 3-COMPONENT | Palladium catalysts | Palladium | Sulfonamides | Acetates | Acids | Transformation | Catalysts | Phosphine | Conversion | Sulfur dioxide | Intermediates | Aromatic compounds | Sulfur | Chemical synthesis | Sulfones | Communications | Communication
oxidation | palladium | sulfur | synthetic methods | electrophiles | SULFONE SYNTHESIS | ONE-POT | DIARYLIODONIUM SALTS | SULFONAMIDES | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | ALKYL-HALIDES | ARYL HALIDES | SULFUR-DIOXIDE SURROGATE | PALLADIUM-CATALYZED AMINOSULFONYLATION | 3-COMPONENT | Palladium catalysts | Palladium | Sulfonamides | Acetates | Acids | Transformation | Catalysts | Phosphine | Conversion | Sulfur dioxide | Intermediates | Aromatic compounds | Sulfur | Chemical synthesis | Sulfones | Communications | Communication
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 06/2015, Volume 13, Issue 24, pp. 6803 - 6813
The direct sulfenylation and sulfonylation of (sp(2))C-H bonds of benzamide derivatives were achieved using a Ni catalyst with the aid of an 8-aminoquinoline...
DIRECTING GROUP | ACID-DERIVATIVES | DIRECT ARYLATION | AROMATIC CARBOXAMIDES | C(SP)-H BOND | COUPLING REACTIONS | UNSYMMETRICAL DIARYL SULFONES | ALKYLATION | ARYL HALIDES | CHEMISTRY, ORGANIC | SULFENYLATION | Aminoquinolines - chemical synthesis | Nickel - chemistry | Sulfones - chemistry | Aminoquinolines - chemistry | Sulfides - chemistry | Models, Molecular | Sulfides - chemical synthesis | Catalysis | Benzamides - chemical synthesis | Benzamides - chemistry | Sulfones - chemical synthesis
DIRECTING GROUP | ACID-DERIVATIVES | DIRECT ARYLATION | AROMATIC CARBOXAMIDES | C(SP)-H BOND | COUPLING REACTIONS | UNSYMMETRICAL DIARYL SULFONES | ALKYLATION | ARYL HALIDES | CHEMISTRY, ORGANIC | SULFENYLATION | Aminoquinolines - chemical synthesis | Nickel - chemistry | Sulfones - chemistry | Aminoquinolines - chemistry | Sulfides - chemistry | Models, Molecular | Sulfides - chemical synthesis | Catalysis | Benzamides - chemical synthesis | Benzamides - chemistry | Sulfones - chemical synthesis
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 10/2017, Volume 82, Issue 19, pp. 10628 - 10634
An efficient one-pot multistep strategy has been developed, comprising auto-oxidative difunctionalization of alkenes, oxidation of sulfides, and a further...
HYDROXY SULFONES | ALKENES | KETO-SULFONES | REDUCTION | WITTIG REACTION | HYDROXYSULFENYLATION | CHEMISTRY, ORGANIC | BOND FORMATION | METAL-FREE | SOLVENT | MOLECULAR-OXYGEN | Tosyl Compounds - chemical synthesis | Sulfones - chemistry | Antineoplastic Agents - chemical synthesis | Anilides - chemistry | Nitriles - chemistry | Models, Molecular | Nitriles - chemical synthesis | Tosyl Compounds - chemistry | Molecular Structure | Antineoplastic Agents - chemistry | Anilides - chemical synthesis | Sulfones - chemical synthesis | Usage | Bicalutamide | Research | Chemical synthesis | Index Medicus
HYDROXY SULFONES | ALKENES | KETO-SULFONES | REDUCTION | WITTIG REACTION | HYDROXYSULFENYLATION | CHEMISTRY, ORGANIC | BOND FORMATION | METAL-FREE | SOLVENT | MOLECULAR-OXYGEN | Tosyl Compounds - chemical synthesis | Sulfones - chemistry | Antineoplastic Agents - chemical synthesis | Anilides - chemistry | Nitriles - chemistry | Models, Molecular | Nitriles - chemical synthesis | Tosyl Compounds - chemistry | Molecular Structure | Antineoplastic Agents - chemistry | Anilides - chemical synthesis | Sulfones - chemical synthesis | Usage | Bicalutamide | Research | Chemical synthesis | Index Medicus
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2018, Volume 57, Issue 7, pp. 1939 - 1943
Thionyl tetrafluoride (SOF4) is a valuable connective gas for sulfur fluoride exchange (SuFEx) click chemistry that enables multidimensional linkages to be...
click chemistry | sulfonimidoyl fluorides | thionyl tetrafluoride | SuFEx chemistry | organolithium reagents | HALIDES | SULFONYL FLUORIDES | POLYSULFATES | ARYL FLUOROSULFATE | SULFINAMIDES | ONE-POT SYNTHESIS | ETHENESULFONYL FLUORIDE | CHEMISTRY, MULTIDISCIPLINARY | ELECTROPHILIC NH | INHIBITORS | Fluorides - chemistry | Lactones - chemical synthesis | Imides - chemistry | Sulfones - chemistry | Imides - chemical synthesis | Organometallic Compounds - chemistry | Lactones - chemistry | Sulfur compounds | Fluorides | Connectors | Chemistry | Fluoride | Chemical bonds | Nitrogen | Sulfur | Nucleophiles | Chemical synthesis | SOF4 | Click Chemistry | SuFEx reaction | Sulfonimidoyl Fluoride | Organolithium
click chemistry | sulfonimidoyl fluorides | thionyl tetrafluoride | SuFEx chemistry | organolithium reagents | HALIDES | SULFONYL FLUORIDES | POLYSULFATES | ARYL FLUOROSULFATE | SULFINAMIDES | ONE-POT SYNTHESIS | ETHENESULFONYL FLUORIDE | CHEMISTRY, MULTIDISCIPLINARY | ELECTROPHILIC NH | INHIBITORS | Fluorides - chemistry | Lactones - chemical synthesis | Imides - chemistry | Sulfones - chemistry | Imides - chemical synthesis | Organometallic Compounds - chemistry | Lactones - chemistry | Sulfur compounds | Fluorides | Connectors | Chemistry | Fluoride | Chemical bonds | Nitrogen | Sulfur | Nucleophiles | Chemical synthesis | SOF4 | Click Chemistry | SuFEx reaction | Sulfonimidoyl Fluoride | Organolithium
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 04/2014, Volume 53, Issue 17, pp. 4404 - 4407
The development of a gold(I)‐catalyzed sulfination of aryl boronic acids is described. This transformation proceeds through an unprecedented mechanism which...
gold | sulfonamides | structure elucidation | heterocycles | synthetic methods | SULFUR-DIOXIDE | COMPLEXES | REACTIVITY | SULFONES | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | AMINOSULFONYLATION | BORONIC ACIDS | ARYL | INHIBITORS | Gold - chemistry | Sulfonamides - chemical synthesis | X-Ray Diffraction | Organometallic Compounds - chemistry | Boronic Acids - chemistry | Molecular Structure | Catalysis | Sulfones - chemical synthesis | Sulfonamides | Pharmaceutical industry | Drugs | Anions | Synthesis | Aromatic compounds | Metalorganic compounds | X-rays | Transformations | Derivatives | Sulfones
gold | sulfonamides | structure elucidation | heterocycles | synthetic methods | SULFUR-DIOXIDE | COMPLEXES | REACTIVITY | SULFONES | CHEMISTRY, MULTIDISCIPLINARY | ARYLBORONIC ACIDS | AMINOSULFONYLATION | BORONIC ACIDS | ARYL | INHIBITORS | Gold - chemistry | Sulfonamides - chemical synthesis | X-Ray Diffraction | Organometallic Compounds - chemistry | Boronic Acids - chemistry | Molecular Structure | Catalysis | Sulfones - chemical synthesis | Sulfonamides | Pharmaceutical industry | Drugs | Anions | Synthesis | Aromatic compounds | Metalorganic compounds | X-rays | Transformations | Derivatives | Sulfones
Journal Article