Suchergebnisse - "Amines chemical synthesis"

Novel bis-arylalkylamines as myeloperoxidase inhibitors: Design, synthesis, and structure-activity relationship study

Autoren: Aldib, Iyas Gelbcke, Michel Soubhye, Jalal et al.

Weitere Verfasser: Aldib, Iyas Gelbcke, Michel Soubhye, Jalal et al.

Quelle: Aldib, I, Gelbcke, M, Soubhye, J, Prévost, M, Furtmüller, P G, Obinger, C, Elfving, B, Alard, I C, Roos, G, Delporte, C, Berger, G, Dufour, D, Zouaoui Boudjeltia, K, Nève, J, Dufrasne, F & Van Antwerpen, P 2016, 'Novel bis-arylalkylamines as myeloperoxidase inhibitors : Design, synthesis, and structure-activity relationship study', European Journal of Medicinal Chemistry, vol. 123, pp. 746-62. https://doi.org/10.1016/j.ejmech.2016.07.053

Schlagwörter: 0301 basic medicine, Halogenation, Protein Conformation, Serotonin Uptake Inhibitors -- chemical synthesis -- chemistry -- metabolism -- pharmacology, [CHIM.THER] Chemical Sciences/Medicinal Chemistry, [CHIM.THER]Chemical Sciences/Medicinal Chemistry, Chemistry Techniques, Synthetic, Docking, Structure-Activity Relationship, 03 medical and health sciences, [CHIM] Chemical Sciences, Journal Article, [CHIM]Chemical Sciences, Humans, Amines, Enzyme Inhibitors, Chimie pharmaceutique, Bis-arylalkylamines derivatives, Peroxidase, Myeloperoxidase selective inhibitors, 0303 health sciences, Peroxidase -- antagonists & inhibitors -- chemistry -- metabolism, SERT, Synthetic, Reversible inhibitors, Chemistry Techniques, 3. Good health, Molecular Docking Simulation, Chimie organique, Kinetics, Drug Design, Pharmacomodulation, Amines -- chemical synthesis -- chemistry -- metabolism -- pharmacology, Enzyme Inhibitors -- chemical synthesis -- chemistry -- metabolism -- pharmacology, Oxidation-Reduction, Selective Serotonin Reuptake Inhibitors

Dateibeschreibung: 1 full-text file(s): application/pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/27537923
https://difusion.ulb.ac.be/vufind/Record/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/235321/Details
http://di.umons.ac.be/details.aspx?pub=f79f05f8-466f-4ffe-8c4f-19b8f7a7ad56
https://www.sciencedirect.com/science/article/pii/S022352341630616X
https://hal.archives-ouvertes.fr/hal-02393046
https://europepmc.org/article/MED/27537923
https://core.ac.uk/display/77592369

Palladium‐Catalyzed Amination of Aryl Sulfides with Anilines

Autoren: Sugahara, Tomohiro Murakami, Kei Yorimitsu, Hideki et al.

Weitere Verfasser: Sugahara, Tomohiro Murakami, Kei Yorimitsu, Hideki et al.

Quelle: Angewandte Chemie. 126:9483-9487

Schlagwörter: aryl sulfides, Amines/chemical synthesis, Sulfides, 7. Clean energy, 01 natural sciences, Catalysis, Heterocyclic Compounds, Palladium/chemistry, Methane/chemistry, Organometallic Compounds, Aniline Compounds/chemistry, N-heterocyclic carbene ligands, Amines, Amines/chemistry, Amination, Aniline Compounds, Molecular Structure, Heterocyclic Compounds/chemistry, Organometallic Compounds/chemistry, Methane/analogs & derivatives, amination, palladium, 3. Good health, 0104 chemical sciences, 13. Climate action, Sulfides/chemistry, Methane, Pummerer reaction, Palladium

Dateibeschreibung: application/pdf

Zugangs-URL: https://repository.kulib.kyoto-u.ac.jp/dspace/bitstream/2433/198446/1/anie.201404355.pdf
https://pubmed.ncbi.nlm.nih.gov/25044919
http://onlinelibrary.wiley.com/doi/10.1002/chin.201507087/abstract
https://pubmed.ncbi.nlm.nih.gov/25044919/
http://ci.nii.ac.jp/naid/120005615640
https://repository.kulib.kyoto-u.ac.jp/dspace/handle/2433/198446
https://ci.nii.ac.jp/naid/120005615640
https://core.ac.uk/display/39321799
https://www.ncbi.nlm.nih.gov/pubmed/25044919

Click Chemistry Facilitates Formation of Reporter Ions and Simplified Synthesis of Amine-Reactive Multiplexed Isobaric Tags for Protein Quantification

Autoren: Raymond J. Deshaies J. Eugene Lee Jesse L. Beauchamp et al.

Quelle: Sohn, C H, Lee, J E, Sweredoski, M J, Graham, R L J, Smith, G T, Hess, S, Czerwieniec, G, Loo, J A, Deshaies, R J & Beauchamp, J L 2012, 'Click chemistry facilitates formation of reporter ions and simplified synthesis of amine-reactive multiplexed isobaric tags for protein quantification', Journal of the American Chemical Society, vol. 134, no. 5, pp. 2672-2680. https://doi.org/10.1021/ja2099003

Schlagwörter: Ions, 0301 basic medicine, 0303 health sciences, Molecular Structure, Amines/chemical synthesis, Proteins, Ions/chemical synthesis, 03 medical and health sciences, Quantum Theory, Click Chemistry, Amines, Proteins/analysis

Zugangs-URL: https://europepmc.org/articles/pmc3668889?pdf=render
https://pubmed.ncbi.nlm.nih.gov/22225568
https://research.manchester.ac.uk/en/publications/e77f55af-9a21-4895-9547-3cb7044513a4
https://doi.org/10.1021/ja2099003
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3668889/
https://yonsei.pure.elsevier.com/en/publications/click-chemistry-facilitates-formation-of-reporter-ions-and-simpli
https://pubs.acs.org/doi/10.1021/ja2099003
https://pubmed.ncbi.nlm.nih.gov/22225568/
http://europepmc.org/articles/PMC3668889

Stereoselective synthesis of N-aryl proline amides by biotransformation–Ugi-Smiles sequence

Autoren: Znabet, Anass Blanken, Sara Janssen, Elwin et al.

Quelle: Znabet, A, Blanken, S, Janssen, E, De Kanter, F J J, Helliwell, M, Turner, N J, Ruijter, E & Orru, R V A 2012, 'Stereoselective synthesis of N-aryl proline amides by biotransformation-Ugi-Smiles sequence', Organic and Biomolecular Chemistry, vol. 10, no. 5, pp. 941-944. https://doi.org/10.1039/c1ob06699d

Schlagwörter: Models, Molecular, Proline, Amines/chemical synthesis, Molecular, Proline/chemical synthesis, Stereoisomerism, Amides, 01 natural sciences, Catalysis, 0104 chemical sciences, Models, Cyclization, ResearchInstitutes_Networks_Beacons/manchester_institute_of_biotechnology, name=Manchester Institute of Biotechnology, Manchester Institute of Biotechnology, Amides/chemical synthesis, Amines, SDG 6 - Clean Water and Sanitation

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/22179495
https://research.vu.nl/en/publications/719685dc-a963-40f2-9ea4-62e0ec4b2685
https://doi.org/10.1039/c1ob06699d
https://hdl.handle.net/1871.1/719685dc-a963-40f2-9ea4-62e0ec4b2685
https://pubs.rsc.org/en/content/articlelanding/2012/ob/c1ob06699d#!
https://www.narcis.nl/publication/RecordID/oai%3Aresearch.vu.nl%3Apublications%2F719685dc-a963-40f2-9ea4-62e0ec4b2685
https://europepmc.org/abstract/MED/22179495
https://www.ncbi.nlm.nih.gov/pubmed/22179495
https://www.research.manchester.ac.uk/portal/en/publications/stereoselective-synthesis-of-naryl-proline-amides-by-biotransformation-ugismiles-sequence(4221d7ae-38ab-4f38-ad23-01678cadade2).html
https://research.vu.nl/en/publications/stereoselective-synthesis-of-n-aryl-proline-amides-by-biotransfor
http://www.scopus.com/inward/record.url?scp=84856755472&partnerID=8YFLogxK
https://doi.org/10.1039/c1ob06699d
https://research.manchester.ac.uk/en/publications/4221d7ae-38ab-4f38-ad23-01678cadade2

Highly Efficient and Diastereoselective Gold(I)‐Catalyzed Synthesis of Tertiary Amines from Secondary Amines and Alkynes: Substrate Scope and Mechanistic Insights

Autoren: Dong, SS Liu, XY Che, CM et al.

Quelle: Chemistry – A European Journal. 17:12932-12945

Schlagwörter: Gold - Chemistry, Molecular Structure, Stereoisomerism, Amines - Chemical Synthesis - Chemistry, 01 natural sciences, Catalysis, 0104 chemical sciences, Alkynes, 0103 physical sciences, Gold, Hydrogenation, Alkynes - Chemistry, Amines

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/22012740
https://www.ncbi.nlm.nih.gov/pubmed/22012740
https://onlinelibrary.wiley.com/doi/full/10.1002/chem.201101982
https://hub.hku.hk/handle/10722/168581
https://experts.umn.edu/en/publications/highly-efficient-and-diastereoselective-goldi-catalyzed-synthesis
https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.201101982
https://core.ac.uk/display/37992969
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchin.201213134
http://onlinelibrary.wiley.com/doi/10.1002/chin.201213134/abstract
http://hdl.handle.net/10722/168581

Secondary Amine Formation from Reductive Amination of Carbonyl Compounds Promoted by Lewis Acid Using the InCl3/Et3SiH System

Autoren: Law, KL Lee, OY Yang, D

Quelle: Organic Letters. 11:3302-3305

Schlagwörter: Aldehydes, Indium - Chemistry, Zinc Compounds - Chemistry, Zinc Compounds, Amines - Chemical Synthesis, Amines, Ketones, Aldehydes - Chemistry, Indium, 01 natural sciences, Ketones - Chemistry, Amination, 0104 chemical sciences

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/19591453
https://onlinelibrary.wiley.com/doi/full/10.1002/chin.200948073
https://pubs.acs.org/doi/10.1021/ol901111g
http://hub.hku.hk/handle/10722/168395
https://europepmc.org/article/MED/19591453
https://www.ncbi.nlm.nih.gov/pubmed/19591453
https://pubs.acs.org/doi/abs/10.1021/ol901111g
http://hdl.handle.net/10722/168395

Spectroscopic Studies and Structures oftrans-Ruthenium(II) and Ruthenium(III) Bis(cyanide) Complexes Supported by a Tetradentate Macrocyclic Tertiary Amine Ligand

Autoren: Yung, FC Zhu, N Che, CM et al.

Quelle: Inorganic Chemistry. 47:10308-10316

Schlagwörter: Macrocyclic Compounds, Organometallic Compounds - Chemical Synthesis - Chemistry, 02 engineering and technology, Crystallography, X-Ray, Ligands, Spectrum Analysis, Raman, 01 natural sciences, Ruthenium, Macrocyclic Compounds - Chemical Synthesis - Chemistry, Electrochemistry, Organometallic Compounds, Amines, Raman, Ultraviolet, Crystallography, Cyanides, Spectrum Analysis, Amines - Chemical Synthesis - Chemistry, 0104 chemical sciences, Spectrophotometry, X-Ray, Cyanides - Chemical Synthesis - Chemistry, Spectrophotometry, Ultraviolet, 0210 nano-technology, Ruthenium - Chemistry

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/18850698
https://www.ncbi.nlm.nih.gov/pubmed/18850698
https://pubs.acs.org/doi/10.1021/ic800743a
http://hub.hku.hk/handle/10722/168346
https://core.ac.uk/display/37992551
https://pubs.acs.org/doi/abs/10.1021/ic800743a
http://www.crystallography.net/cod/4305799.html
http://hdl.handle.net/10722/168346

Physicochemical Investigation of a Lipid with a New Core Structure for Gene Transfection: 2-Amino-3-hexadecyloxy-2-(hexadecyloxymethyl)propan-1-ol

Autoren: Antipina, M. N. Schulze, I. Dobner, B. et al.

Quelle: Langmuir 23, 3926 (2007). doi:10.1021/la062840i

Schlagwörter: Lipids: chemical synthesis, Propanols, DNA, 02 engineering and technology, Transfection, Lipids, 01 natural sciences, Propanols: chemistry, Amines: chemical synthesis, Amines: chemistry, 0104 chemical sciences, DNA: chemistry, Lipids: chemistry, Liposomes, Amines, 0210 nano-technology, Propanols: chemical synthesis, 2-amino-3-hexadecyloxy-2-(hexadecyloxymethyl)propan-1-ol

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/17309283
https://core.ac.uk/display/20501263
https://www.ncbi.nlm.nih.gov/pubmed/17309283
http://pubman.mpdl.mpg.de/pubman/item/escidoc:1927769
https://pubs.acs.org/doi/10.1021/la062840i
https://pure.mpg.de/pubman/faces/ViewItemOverviewPage.jsp?itemId=item_1927769
https://bib-pubdb1.desy.de/record/82201

Synthesis and tissue distribution of four Se-labeled tertiary amines, potential brain pH imaging agents

Autoren: Plenevaux, Alain Cantineau, Robert Brihaye, Claude et al.

Weitere Verfasser: Plenevaux, Alain Cantineau, Robert Brihaye, Claude et al.

Quelle: International Journal of Radiation Applications and Instrumentation. Part B. Nuclear Medicine and Biology. 17:601-607

Schlagwörter: Amines/chemical synthesis/pharmacokinetics, Brain Chemistry, Selenium Radioisotopes, Radiologie, médecine & imagerie nucléaire, Hydrogen-Ion Concentration, Sciences de la santé humaine, Rats, Selenium, 03 medical and health sciences, Selenium/pharmacokinetics, 0302 clinical medicine, Selenium Radioisotopes/diagnostic use, Animals, Female, Tissue Distribution, Human health sciences, Amines, Radiology, nuclear medicine & imaging

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/2254097
https://orbi.uliege.be/handle/2268/5261
http://orbi.ulg.ac.be/handle/2268/5261
https://europepmc.org/article/MED/2254097
https://www.sciencedirect.com/science/article/pii/088328979090136O
https://hdl.handle.net/2268/5261
https://doi.org/10.1016/0883-2897(90)90136-O

Alkylsquarates as key intermediates for the rapid preparation of original drug-inspired compounds.

Autoren: Charton, Julie Charruault, Lise Déprez-Poulain, Rebecca et al.

Weitere Verfasser: Charton, Julie Charruault, Lise Déprez-Poulain, Rebecca et al.

Quelle: ISSN: 1386-2073 ; Combinatorial Chemistry and High Throughput Screening ; https://inserm.hal.science/inserm-00281198 ; Combinatorial Chemistry and High Throughput Screening, 2008, 11 (4), pp.294-303. ⟨10.2174/138620708784246013⟩.

Schlagwörter: MESH: Amines/chemical synthesis, MESH: Amines/chemistry, MESH: Chelating Agents/chemical synthesis, MESH: Chelating Agents/chemistry, MESH: Chemistry, Pharmaceutical/methods, MESH: Combinatorial Chemistry Techniques/methods, MESH: Cyclobutanes/chemistry, MESH: Enzyme Inhibitors/chemical synthesis, MESH: Enzyme Inhibitors/chemistry, MESH: Esters/chemistry, MESH: Hydroxamic Acids/chemistry, MESH: Molecular Structure, MESH: Pharmaceutical Preparations/chemical synthesis, MESH: Pharmaceutical Preparations/chemistry, MESH: Piperidines/chemistry, MESH: Small Molecule Libraries/chemical synthesis, MESH: Small Molecule Libraries/chemistry, MESH: Zinc/chemistry, [SDV.SP]Life Sciences [q-bio]/Pharmaceutical sciences

Relation: info:eu-repo/semantics/altIdentifier/pmid/18473739; PUBMED: 18473739

Verfügbarkeit: https://inserm.hal.science/inserm-00281198
https://inserm.hal.science/inserm-00281198v1/document
https://inserm.hal.science/inserm-00281198v1/file/CCHTS-Charton_et_al.pdf
https://doi.org/10.2174/138620708784246013

ChemInform Abstract: Highly Enantioselective Synthesis of Chiral Secondary Amines by Gold(I)/Chiral Broensted Acid Catalyzed Tandem Intermolecular Hydroamination and Transfer Hydrogenation Reactions

Autoren: Liu, XY Che, CM

Quelle: ChemInform. 41

Schlagwörter: Amines - chemical synthesis, Aniline Compounds, Molecular Structure, Stereoisomerism, 01 natural sciences, Catalysis, 0104 chemical sciences, Gold - chemistry, Cyclization, Alkynes - chemistry, Alkynes, Aniline Compounds - chemistry, Gold, Hydrogenation, Amines

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/19678678
https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fchin.201006067
http://onlinelibrary.wiley.com/doi/10.1002/chin.201006067/full
https://pubs.acs.org/doi/10.1021/ol901443b
https://europepmc.org/abstract/MED/19678678
https://pubs.acs.org/doi/abs/10.1021/ol901443b
https://core.ac.uk/display/153025157
http://hub.hku.hk/handle/10722/70254
https://www.ncbi.nlm.nih.gov/pubmed/19678678
http://hdl.handle.net/10722/70254

Highly enantioselective synthesis of chiral secondary amines by gold(I)/ chiral bronsted acid catalyzed tandem intermodular hydroamination and transfer hydrogenation reactions

Autoren: Liu, XY Che, CM

Schlagwörter: Amines - chemical synthesis, Alkynes - chemistry, Stereoisomerism, Gold - chemistry, Aniline Compounds - chemistry

Relation: Organic Letters; Institute of molecular technology for drug discovery and synthesis; http://www.scopus.com/mlt/select.url?eid=2-s2.0-70349147881&selection=ref&src=s&origin=recordpage; 9067278; 4207; 168981; WOS:000269670700045; 18; 4204; http://hdl.handle.net/10722/70254; 11

Verfügbarkeit: https://doi.org/10.1021/ol901443b
http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1523-7060&volume=11&issue=18&spage=4204&epage=4207&date=2009&atitle=Highly+enantioselective+synthesis+of+chiral+secondary+amines+by+gold+(I)/+chiral+Brønsted+acid+catalyzed+tandem+intermolecular+hydroamination+and+transfer+hydrogenation+reactions
http://hdl.handle.net/10722/70254

Palladium-catalyzed amination of aryl sulfides with anilines.

Autoren: Murakami, Kei Yorimitsu, Hideki Osuka, Atsuhiro et al.

Index Begriffe: amination, aryl sulfides, N-heterocyclic carbene ligands, palladium, Pummerer reaction, Amination, Amines/chemical synthesis, Amines/chemistry, Aniline Compounds/chemistry, Catalysis, Heterocyclic Compounds/chemistry, Methane/analogs & derivatives, Methane/chemistry, Molecular Structure, Organometallic Compounds/chemistry, Palladium/chemistry, Sulfides/chemistry, Journal Article., AM.

URL: http://hdl.handle.net/2433/198446
http://repository.kulib.kyoto-u.ac.jp/dspace/bitstream/2433/198446/1/anie.201404355.pdf
25044919