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Wyszukujesz frazę ""Halogenation"" wg kryterium: Temat


Tytuł :
A Unified Approach to Decarboxylative Halogenation of (Hetero)aryl Carboxylic Acids.
Autorzy :
Chen TQ; Merck Center for Catalysis at Princeton University, Princeton, New Jersey 08544, United States.
Pedersen PS; Merck Center for Catalysis at Princeton University, Princeton, New Jersey 08544, United States.
Dow NW; Merck Center for Catalysis at Princeton University, Princeton, New Jersey 08544, United States.
Fayad R; Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695, United States.
Hauke CE; Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695, United States.
Rosko MC; Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695, United States.
Danilov EO; Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695, United States.
Blakemore DC; Worldwide Research and Development, Pfizer, Inc., Eastern Point Road, Groton, Connecticut 06340, United States.
Dechert-Schmitt AM; Worldwide Research and Development, Pfizer, Inc., Eastern Point Road, Groton, Connecticut 06340, United States.
Knauber T; Worldwide Research and Development, Pfizer, Inc., Eastern Point Road, Groton, Connecticut 06340, United States.
Castellano FN; Department of Chemistry, North Carolina State University, Raleigh, North Carolina 27695, United States.
MacMillan DWC; Merck Center for Catalysis at Princeton University, Princeton, New Jersey 08544, United States.
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Źródło :
Journal of the American Chemical Society [J Am Chem Soc] 2022 May 11; Vol. 144 (18), pp. 8296-8305. Date of Electronic Publication: 2022 Apr 29.
Typ publikacji :
Journal Article
MeSH Terms :
Carboxylic Acids*/chemistry
Halogenation*
Catalysis ; Copper/chemistry ; Ligands
Czasopismo naukowe
Tytuł :
Synthesis of 1 H -isoindoliums by electrophile-mediated cascade cyclization/iodination of propargylamine-based 1,6-diynes.
Autorzy :
Cui JF; Department of Chemistry, Southern University of Science and Technology, 1088 Xueyuan Blvd., Shenzhen 518055, China.
Yu Q; The Hong Kong Polytechnic University Shenzhen Research Institute, Shenzhen 518057, China.
O WY; State Key Laboratory of Chemical Biology and Drug Discovery, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Hong Kong, China. .; The Hong Kong Polytechnic University Shenzhen Research Institute, Shenzhen 518057, China.
Huang LW; The Hong Kong Polytechnic University Shenzhen Research Institute, Shenzhen 518057, China.
Yang B; State Key Laboratory of Chemical Biology and Drug Discovery, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Hong Kong, China. .
Wong MK; State Key Laboratory of Chemical Biology and Drug Discovery, Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Hong Kong, China. .; The Hong Kong Polytechnic University Shenzhen Research Institute, Shenzhen 518057, China.
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Źródło :
Organic & biomolecular chemistry [Org Biomol Chem] 2022 May 11; Vol. 20 (18), pp. 3755-3762. Date of Electronic Publication: 2022 May 11.
Typ publikacji :
Journal Article
MeSH Terms :
Diynes*
Halogenation*
Catalysis ; Cyclization ; Molecular Structure ; Pargyline/analogs & derivatives ; Propylamines
Czasopismo naukowe
Tytuł :
Structural and Functional Insights into a Nonheme Iron- and α-Ketoglutarate-Dependent Halogenase That Catalyzes Chlorination of Nucleotide Substrates.
Autorzy :
Dai L; State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Hongshan Laboratory, Hubei Collaborative Innovation Center for Green Transformation of Bio-Resources, Hubei Key Laboratory of Industrial Biotechnology, School of Life Sciences, Hubei University, Wuhan, People's Republic of China.
Zhang X; State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Hongshan Laboratory, Hubei Collaborative Innovation Center for Green Transformation of Bio-Resources, Hubei Key Laboratory of Industrial Biotechnology, School of Life Sciences, Hubei University, Wuhan, People's Republic of China.
Hu Y; State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Hongshan Laboratory, Hubei Collaborative Innovation Center for Green Transformation of Bio-Resources, Hubei Key Laboratory of Industrial Biotechnology, School of Life Sciences, Hubei University, Wuhan, People's Republic of China.
Shen J; State Key Laboratory of Virology, College of Life Sciences, Wuhan Universitygrid.49470.3e, Wuhan, People's Republic of China.
Zhang Q; State Key Laboratory of Virology, College of Life Sciences, Wuhan Universitygrid.49470.3e, Wuhan, People's Republic of China.
Zhang L; State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Hongshan Laboratory, Hubei Collaborative Innovation Center for Green Transformation of Bio-Resources, Hubei Key Laboratory of Industrial Biotechnology, School of Life Sciences, Hubei University, Wuhan, People's Republic of China.
Min J; State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Hongshan Laboratory, Hubei Collaborative Innovation Center for Green Transformation of Bio-Resources, Hubei Key Laboratory of Industrial Biotechnology, School of Life Sciences, Hubei University, Wuhan, People's Republic of China.
Chen CC; State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Hongshan Laboratory, Hubei Collaborative Innovation Center for Green Transformation of Bio-Resources, Hubei Key Laboratory of Industrial Biotechnology, School of Life Sciences, Hubei University, Wuhan, People's Republic of China.
Liu Y; State Key Laboratory of Virology, College of Life Sciences, Wuhan Universitygrid.49470.3e, Wuhan, People's Republic of China.
Huang JW; State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Hongshan Laboratory, Hubei Collaborative Innovation Center for Green Transformation of Bio-Resources, Hubei Key Laboratory of Industrial Biotechnology, School of Life Sciences, Hubei University, Wuhan, People's Republic of China.
Guo RT; State Key Laboratory of Biocatalysis and Enzyme Engineering, Hubei Hongshan Laboratory, Hubei Collaborative Innovation Center for Green Transformation of Bio-Resources, Hubei Key Laboratory of Industrial Biotechnology, School of Life Sciences, Hubei University, Wuhan, People's Republic of China.
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Źródło :
Applied and environmental microbiology [Appl Environ Microbiol] 2022 May 10; Vol. 88 (9), pp. e0249721. Date of Electronic Publication: 2022 Apr 18.
Typ publikacji :
Journal Article
MeSH Terms :
Halogenation*
Ketoglutaric Acids*
Carrier Proteins ; Ferrous Compounds ; Halogens ; Iron/chemistry ; Molecular Docking Simulation ; Nucleotides
Czasopismo naukowe
Tytuł :
Ring-Opening Fluorination of Isoxazoles.
Autorzy :
Komatsuda M; Department of Applied Chemistry, Waseda University, 513 Wasedatsurumakicho, Shinjuku, Tokyo 162-0041, Japan.
Ohki H; Department of Applied Chemistry, Waseda University, 513 Wasedatsurumakicho, Shinjuku, Tokyo 162-0041, Japan.
Kondo H Jr; Department of Applied Chemistry, Waseda University, 513 Wasedatsurumakicho, Shinjuku, Tokyo 162-0041, Japan.
Suto A; Department of Applied Chemistry, Waseda University, 513 Wasedatsurumakicho, Shinjuku, Tokyo 162-0041, Japan.
Yamaguchi J; Department of Applied Chemistry, Waseda University, 513 Wasedatsurumakicho, Shinjuku, Tokyo 162-0041, Japan.
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Źródło :
Organic letters [Org Lett] 2022 May 06; Vol. 24 (17), pp. 3270-3274. Date of Electronic Publication: 2022 Apr 26.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Fluorine*
Halogenation*
Isoxazoles
Czasopismo naukowe
Tytuł :
anti-Markovnikov Iodofluorination of Alkenes.
Autorzy :
Qian BY; Department of Chemistry, Innovative Drug Research Center, Shanghai University, 99 Shangda Road, Shanghai, 200444, P. R. China.
Zhang W; Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, P. R. China.
Lin JH; Department of Chemistry, Innovative Drug Research Center, Shanghai University, 99 Shangda Road, Shanghai, 200444, P. R. China.; Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, P. R. China.
Cao W; Department of Chemistry, Innovative Drug Research Center, Shanghai University, 99 Shangda Road, Shanghai, 200444, P. R. China.; Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, P. R. China.
Xiao JC; Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Lingling Road, Shanghai, 200032, P. R. China.
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Źródło :
Chemistry, an Asian journal [Chem Asian J] 2022 May 02; Vol. 17 (9), pp. e202200184. Date of Electronic Publication: 2022 Mar 22.
Typ publikacji :
Journal Article
MeSH Terms :
Alkenes*/chemistry
Halogenation*
Catalysis
Czasopismo naukowe
Tytuł :
Expanding the Chemical Diversity of Fasamycin Via Genome Mining and Biocatalysis.
Autorzy :
Jiang K; State Key Laboratory of Microbial Metabolism & School of Life Sciences and Biotechnology and Joint International Research Laboratory of Metabolic and Developmental Sciences, Shanghai Jiao Tong University, Shanghai 200240, China.
Yan X; State Key Laboratory of Microbial Metabolism & School of Life Sciences and Biotechnology and Joint International Research Laboratory of Metabolic and Developmental Sciences, Shanghai Jiao Tong University, Shanghai 200240, China.
Deng Z; State Key Laboratory of Microbial Metabolism & School of Life Sciences and Biotechnology and Joint International Research Laboratory of Metabolic and Developmental Sciences, Shanghai Jiao Tong University, Shanghai 200240, China.
Lei C; School of Pharmacy, Fudan University, Shanghai 201203, China.
Qu X; State Key Laboratory of Microbial Metabolism & School of Life Sciences and Biotechnology and Joint International Research Laboratory of Metabolic and Developmental Sciences, Shanghai Jiao Tong University, Shanghai 200240, China.
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Źródło :
Journal of natural products [J Nat Prod] 2022 Apr 22; Vol. 85 (4), pp. 943-950. Date of Electronic Publication: 2022 Mar 24.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Bacillus subtilis*
Halogenation*
Anti-Bacterial Agents/chemistry ; Anti-Bacterial Agents/pharmacology ; Biocatalysis ; Staphylococcus aureus
Czasopismo naukowe
Tytuł :
Synthesis of Cyclopropenes and Fluorinated Cyclopropanes via Michael Initiated Ring Closure of Alkyl Triflones.
Autorzy :
Wang H; Key Laboratory of Science and Technology of Eco-Textiles, Ministry of Education, College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai, 201620, P. R. China.
Yang RY; Key Laboratory of Science and Technology of Eco-Textiles, Ministry of Education, College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai, 201620, P. R. China.
Xu B; Key Laboratory of Science and Technology of Eco-Textiles, Ministry of Education, College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai, 201620, P. R. China.
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Źródło :
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2022 Apr 22; Vol. 28 (23), pp. e202104364. Date of Electronic Publication: 2022 Mar 21.
Typ publikacji :
Journal Article
MeSH Terms :
Cyclopropanes*
Halogenation*
Cyclization ; Molecular Structure ; Stereoisomerism
Czasopismo naukowe
Tytuł :
Fluorine-Containing Drug Administration in Rats Results in Fluorination of Selected Proteins in Liver and Brain Tissue.
Autorzy :
Gawor A; Biological and Chemical Research Centre, Faculty of Chemistry, University of Warsaw, Zwirki i Wigury 101, 02-089 Warsaw, Poland.
Gajewski Z; Center for Translational Medicine, Warsaw University of Life Science, Nowoursynowska 100, 02-797 Warsaw, Poland.
Paczek L; Department of Immunology, Transplantology and Internal Diseases, Medical University of Warsaw, Nowogrodzka 59, 02-006 Warsaw, Poland.; Department of Bioinformatics, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawinskiego 5a, 02-106 Warsaw, Poland.
Czarkowska-Paczek B; Department of Clinical Nursing, Medical University of Warsaw, Ciolka Street 27, 01-445 Warsaw, Poland.
Konopka A; Biological and Chemical Research Centre, Faculty of Chemistry, University of Warsaw, Zwirki i Wigury 101, 02-089 Warsaw, Poland.
Wryk G; Biological and Chemical Research Centre, Faculty of Chemistry, University of Warsaw, Zwirki i Wigury 101, 02-089 Warsaw, Poland.
Bulska E; Biological and Chemical Research Centre, Faculty of Chemistry, University of Warsaw, Zwirki i Wigury 101, 02-089 Warsaw, Poland.
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Źródło :
International journal of molecular sciences [Int J Mol Sci] 2022 Apr 11; Vol. 23 (8). Date of Electronic Publication: 2022 Apr 11.
Typ publikacji :
Journal Article
MeSH Terms :
Fluorine*/chemistry
Halogenation*
Animals ; Brain ; Cinacalcet ; Fluorides ; Liver ; Pharmaceutical Preparations ; Rats ; Rats, Wistar ; Spectrin ; Tandem Mass Spectrometry
Czasopismo naukowe
Tytuł :
One-Pot Synthesis of 2,5-Furandicarboxylic Acid from 2-Furoic Acid by a Pd-catalyzed Bromination-Hydroxycarbonylation Tandem Reaction in Acetate Buffer.
Autorzy :
Yao YQ; Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, 200062, Shanghai, China.
Zhao KC; Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, 200062, Shanghai, China.
Zhuang YY; Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, 200062, Shanghai, China.
Chen XC; Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, 200062, Shanghai, China.
Lu Y; Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, 200062, Shanghai, China.
Liu Y; Shanghai Key Laboratory of Green Chemistry and Chemical Processes, School of Chemistry and Molecular Engineering, East China Normal University, 200062, Shanghai, China.
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Źródło :
ChemistryOpen [ChemistryOpen] 2022 Apr; Vol. 11 (4), pp. e202100301.
Typ publikacji :
Journal Article
MeSH Terms :
Halogenation*
Palladium*
Acetates ; Dicarboxylic Acids ; Furans
Czasopismo naukowe
Tytuł :
Synthetic metabolism for biohalogenation.
Autorzy :
Cros A; The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.
Alfaro-Espinoza G; Max Planck Institute of Molecular Plant Physiology, 14476 Potsdam-Golm, Germany; Division Biodeterioration and Reference Organisms, Federal Institute for Materials Research and Testing (BAM), 12205 Berlin, Germany.
De Maria A; The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, 2800 Kongens Lyngby, Denmark; Max Planck Institute of Molecular Plant Physiology, 14476 Potsdam-Golm, Germany.
Wirth NT; The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, 2800 Kongens Lyngby, Denmark.
Nikel PI; The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, 2800 Kongens Lyngby, Denmark. Electronic address: .
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Źródło :
Current opinion in biotechnology [Curr Opin Biotechnol] 2022 Apr; Vol. 74, pp. 180-193. Date of Electronic Publication: 2021 Dec 23.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Bacteria*/metabolism
Halogenation*
Biodegradation, Environmental ; Synthetic Biology
Czasopismo naukowe
Tytuł :
3,6,13,16-Tetrapropylporphycene: Rational Synthesis, Complexation, and Halogenation.
Autorzy :
Nagamaiah J; School of Chemistry, University of Hyderabad, Hyderabad 500046, India.
Dutta A; School of Chemistry, University of Hyderabad, Hyderabad 500046, India.
Pati NN; School of Chemistry, University of Hyderabad, Hyderabad 500046, India.
Sahoo S; School of Chemistry, University of Hyderabad, Hyderabad 500046, India.
Soman R; School of Chemistry, University of Hyderabad, Hyderabad 500046, India.
Panda PK; School of Chemistry, University of Hyderabad, Hyderabad 500046, India.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 Mar 04; Vol. 87 (5), pp. 2721-2729. Date of Electronic Publication: 2022 Jan 21.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Halogenation*
Photochemotherapy*
Fluorescence ; Photosensitizing Agents ; Singlet Oxygen
Czasopismo naukowe
Tytuł :
Fluorination Promotes the Cytosolic Delivery of Genes, Proteins, and Peptides.
Autorzy :
Lv J; Shanghai Frontiers Science Center of Genome Editing and Cell Therapy, Shanghai Key Laboratory of Regulatory Biology, School of Life Sciences, East China Normal University, Shanghai 200241, P. R. China.
Wang H; South China Advanced Institute for Soft Matter Science and Technology, Guangdong Provincial Key Laboratory of Functional and Intelligent Hybrid Materials and Devices, School of Molecular Science and Engineering, South China University of Technology, Guangzhou 510640, P. R. China.
Rong G; South China Advanced Institute for Soft Matter Science and Technology, Guangdong Provincial Key Laboratory of Functional and Intelligent Hybrid Materials and Devices, School of Molecular Science and Engineering, South China University of Technology, Guangzhou 510640, P. R. China.
Cheng Y; Shanghai Frontiers Science Center of Genome Editing and Cell Therapy, Shanghai Key Laboratory of Regulatory Biology, School of Life Sciences, East China Normal University, Shanghai 200241, P. R. China.
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Źródło :
Accounts of chemical research [Acc Chem Res] 2022 Mar 01; Vol. 55 (5), pp. 722-733. Date of Electronic Publication: 2022 Feb 17.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Cell-Penetrating Peptides*/metabolism
Halogenation*
Cytosol/metabolism ; Gene Transfer Techniques ; Proteins/metabolism
Czasopismo naukowe
Tytuł :
S-(Trifluoromethyl)Benzothioate (TFBT): A KF-Based Reagent for Nucleophilic Trifluoromethylthiolation.
Autorzy :
Meng D; Key Laboratory of Organofluorine Chemistry Shanghai Institute of Organic Chemistry University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Ling-Ling Road, Shanghai, 200032, China.
Lyu Y; Key Laboratory of Organofluorine Chemistry Shanghai Institute of Organic Chemistry University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Ling-Ling Road, Shanghai, 200032, China.
Ni C; Key Laboratory of Organofluorine Chemistry Shanghai Institute of Organic Chemistry University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Ling-Ling Road, Shanghai, 200032, China.
Zhou M; Key Laboratory of Organofluorine Chemistry Shanghai Institute of Organic Chemistry University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Ling-Ling Road, Shanghai, 200032, China.
Li Y; School of Chemistry and Chemical Engineering, Chongqing University, Chongqing, 400030, P. R. China.
Hu J; Key Laboratory of Organofluorine Chemistry Shanghai Institute of Organic Chemistry University of Chinese Academy of Sciences, Chinese Academy of Sciences, 345 Ling-Ling Road, Shanghai, 200032, China.
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Źródło :
Chemistry (Weinheim an der Bergstrasse, Germany) [Chemistry] 2022 Mar 01; Vol. 28 (13), pp. e202104395. Date of Electronic Publication: 2022 Feb 11.
Typ publikacji :
Journal Article
MeSH Terms :
Fluorine*
Halogenation*
Alcohols ; Boronic Acids ; Indicators and Reagents
Czasopismo naukowe
Tytuł :
Natural and Synthetic Halogenated Amino Acids-Structural and Bioactive Features in Antimicrobial Peptides and Peptidomimetics.
Autorzy :
Mardirossian M; Department of Medicine, Surgery and Health Sciences, University of Trieste, Piazza dell'Ospitale, 1, 34125 Trieste, Italy.
Rubini M; School of Chemistry, University College Dublin, Belfield, Dublin 4, Ireland.
Adamo MFA; Department of Chemistry, Centre for Synthesis and Chemical Biology (CSCB), RCSI, 123 St. Stephens Green, Dublin 2, Ireland.
Scocchi M; Department of Life Sciences, University of Trieste, Via L. Giorgieri, 5, Q Building, 34127 Trieste, Italy.
Saviano M; Institute of Crystallography (IC), National Research Council (CNR), Via Amendola, 122, 70126 Bari, Italy.
Tossi A; Department of Life Sciences, University of Trieste, Via L. Giorgieri, 5, Q Building, 34127 Trieste, Italy.
Gennaro R; Department of Life Sciences, University of Trieste, Via L. Giorgieri, 5, Q Building, 34127 Trieste, Italy.
Caporale A; Institute of Crystallography (IC), National Research Council (CNR), c/o Area Science Park, S.S. 14 Km 163.5, Basovizza, 34149 Trieste, Italy.
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Źródło :
Molecules (Basel, Switzerland) [Molecules] 2021 Dec 06; Vol. 26 (23). Date of Electronic Publication: 2021 Dec 06.
Typ publikacji :
Journal Article; Review
MeSH Terms :
Halogenation*
Anti-Bacterial Agents/*chemistry
Antimicrobial Peptides/*chemistry
Halogens/*chemistry
Peptidomimetics/*metabolism
Proline/*analogs & derivatives
Anti-Bacterial Agents/pharmacology ; Gram-Negative Bacteria/drug effects ; Gram-Positive Bacteria/drug effects ; Humans ; Microbial Sensitivity Tests ; Peptidomimetics/chemistry ; Peptoids/chemistry ; Proline/chemistry ; Structure-Activity Relationship
Czasopismo naukowe
Tytuł :
Chlorination of soil organic matter: The role of humus type and land use.
Autorzy :
Svensson T; Department of Thematic Studies - Environmental Change, Linköping University, 581 83 Linköping, Sweden. Electronic address: .
Redon PO; Andra, Research and Development Division, 1/7 rue Jean-Monnet, 92298 Chatenay-Malabry Cedex, France.
Thiry Y; Andra, Research and Development Division, 1/7 rue Jean-Monnet, 92298 Chatenay-Malabry Cedex, France.
Montelius M; Swedish Geotechnical Institute (SGI), 581 93 Linköping, Sweden.
Bastviken D; Department of Thematic Studies - Environmental Change, Linköping University, 581 83 Linköping, Sweden.
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Źródło :
The Science of the total environment [Sci Total Environ] 2022 Feb 01; Vol. 806 (Pt 2), pp. 150478. Date of Electronic Publication: 2021 Sep 25.
Typ publikacji :
Journal Article
MeSH Terms :
Halogenation*
Soil*
Agriculture ; Carbon ; Forests
Czasopismo naukowe
Tytuł :
Cu-Catalyzed Site-Selective Benzylic Chlorination Enabling Net C-H Coupling with Oxidatively Sensitive Nucleophiles.
Autorzy :
Lopez MA; Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53706, United States.
Buss JA; Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53706, United States.
Stahl SS; Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, Wisconsin 53706, United States.
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Źródło :
Organic letters [Org Lett] 2022 Jan 21; Vol. 24 (2), pp. 597-601. Date of Electronic Publication: 2021 Dec 29.
Typ publikacji :
Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Halogenation*
Czasopismo naukowe
Tytuł :
Enantioselective Construction of Tertiary α-Alkyl Fluoride via BTM-Catalyzed Fluorination of α-Alkynyl-Substituted Acetic Acids.
Autorzy :
Yuan S; State Key Laboratory of Coordination Chemistry, Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry and Chemical Engineering, Nanjing University, 163 Xianlin Avenue, Nanjing, Jiangsu 210023, China.
Zheng WH; State Key Laboratory of Coordination Chemistry, Jiangsu Key Laboratory of Advanced Organic Materials, School of Chemistry and Chemical Engineering, Nanjing University, 163 Xianlin Avenue, Nanjing, Jiangsu 210023, China.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 Jan 07; Vol. 87 (1), pp. 713-720. Date of Electronic Publication: 2021 Dec 20.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Fluorides*
Halogenation*
Acetates ; Catalysis ; Stereoisomerism
Czasopismo naukowe
Tytuł :
Enantioenriched γ-Aminoalcohols, β-Amino Acids, β-Lactams, and Azetidines Featuring Tetrasubstituted Fluorinated Stereocenters via Palladacycle-Catalyzed Asymmetric Fluorination of Isoxazolinones.
Autorzy :
Wannenmacher N; Institut für Organische Chemie, Universität Stuttgart, Pfaffenwaldring 55, D-70569 Stuttgart, Germany.
Pfeffer C; Institut für Organische Chemie, Universität Stuttgart, Pfaffenwaldring 55, D-70569 Stuttgart, Germany.
Frey W; Institut für Organische Chemie, Universität Stuttgart, Pfaffenwaldring 55, D-70569 Stuttgart, Germany.
Peters R; Institut für Organische Chemie, Universität Stuttgart, Pfaffenwaldring 55, D-70569 Stuttgart, Germany.
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Źródło :
The Journal of organic chemistry [J Org Chem] 2022 Jan 07; Vol. 87 (1), pp. 670-682. Date of Electronic Publication: 2021 Dec 10.
Typ publikacji :
Journal Article
MeSH Terms :
Azetidines*
Halogenation*
Amino Acids ; Catalysis ; Stereoisomerism ; beta-Lactams
Czasopismo naukowe
Tytuł :
Comparing the effect of independent and combined interventions of household chlorination and handwashing on diarrhea of under-fives in rural Dire Dawa, Eastern Ethiopia: a cluster randomized controlled trial.
Autorzy :
Solomon ET; Ethiopian Institute of Water Resources, Addis Ababa University, Addis Ababa, Ethiopia.; University of California, San Francisco Medical Center, San Francisco, California, United States of America.
Gari SR; Ethiopian Institute of Water Resources, Addis Ababa University, Addis Ababa, Ethiopia.
Kloos H; Haramaya University, College of Health and Medical Sciences, Harar, Ethiopia.
Alemu BM; University of California, San Francisco Medical Center, San Francisco, California, United States of America.
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Źródło :
The Pan African medical journal [Pan Afr Med J] 2021 Dec 20; Vol. 40, pp. 239. Date of Electronic Publication: 2021 Dec 20 (Print Publication: 2021).
Typ publikacji :
Journal Article; Randomized Controlled Trial
MeSH Terms :
Halogenation*
Hand Disinfection*
Child ; Diarrhea/epidemiology ; Diarrhea/prevention & control ; Ethiopia/epidemiology ; Humans ; Sanitation
Czasopismo naukowe
Tytuł :
Influence of Methylene Fluorination and Chain Length on the Hydration Shell Structure and Thermodynamics of Linear Diols.
Autorzy :
Robalo JR; Department of Theory & Bio-systems, Max Planck Institute for Colloids and Interfaces, Science Park, Potsdam 14476, Germany.
Mendes de Oliveira D; Purdue University, Department of Chemistry, West Lafayette, Indiana 47907, United States.
Ben-Amotz D; Purdue University, Department of Chemistry, West Lafayette, Indiana 47907, United States.
Vila Verde A; University of Duisburg-Essen, Faculty of Physics, Lotharstrasse 1, 47057 Duisburg, Germany.
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Źródło :
The journal of physical chemistry. B [J Phys Chem B] 2021 Dec 16; Vol. 125 (49), pp. 13552-13564. Date of Electronic Publication: 2021 Dec 07.
Typ publikacji :
Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
MeSH Terms :
Halogenation*
Water*
Hydrogen Bonding ; Hydrophobic and Hydrophilic Interactions ; Solutions ; Thermodynamics
Czasopismo naukowe

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