المؤلفون: Hao Song (383912), Yao Xiao (227567), Zhuohua Zhang (77108), Wanjin Xiong (11880001), Ren Wang (188650), Liangcheng Guo (11880004), Taigang Zhou (1474651)

مصطلحات موضوعية: Biochemistry, Genetics, Molecular Biology, Pharmacology, Biotechnology, Evolutionary Biology, Cancer, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, oxazaborolidine – bh, catalyzed transfer hydrogenation, 40 secondary amines, 30 primary amine, 3 , 15 , secondary amines, primary amine, synthesized via, selectivity control, n labeled, mild conditions, high selectivity, 95 %

Relation: https://figshare.com/articles/journal_contribution/Switching_Selectivity_in_Copper-Catalyzed_Transfer_Hydrogenation_of_Nitriles_to_Primary_Amine-Boranes_and_Secondary_Amines_under_Mild_Conditions/17695753

الاتاحة: https://doi.org/10.1021/acs.joc.1c02413.s001

المؤلفون: Qi Guo (133147), Jingchao Chen (1533052), Guoli Shen (12078), Guangfu Lu (11571485), Xuemei Yang (40623), Yan Tang (195081), Yuanbin Zhu (11401191), Shiyuan Wu (10699929), Baomin Fan (1490236)

مصطلحات موضوعية: Microbiology, Genetics, Evolutionary Biology, Cancer, Computational Biology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, free environmentally benign, catalyzed transfer hydrogenation, 4 , tetrabutylammonium bromide, quinoxalines offering, hydrogen source, excellent yields, developed using, desired tetrahydroquinoxalines, cost catalyst

Relation: https://figshare.com/articles/journal_contribution/Tetrabutylammonium_Bromide-Catalyzed_Transfer_Hydrogenation_of_Quinoxaline_with_HBpin_as_a_Hydrogen_Source/17203666

الاتاحة: https://doi.org/10.1021/acs.joc.1c02537.s001

المؤلفون: Hayes, Joseph M., Deydier, Éric, Ujaque, Gregori, Lledos, Agusti, Malacea-Kabbara, Raluca, Manoury, E., Vincendeau, Sandrine, Poli, Rinaldo

المساهمون: Departament de Química Barcelona (UAB), Universitat Autònoma de Barcelona = Autonomous University of Barcelona = Universidad Autónoma de Barcelona (UAB), Laboratoire de chimie de coordination (LCC), Institut de Chimie de Toulouse (ICT), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Institut universitaire de France (IUF), Ministère de l'Education nationale, de l’Enseignement supérieur et de la Recherche (M.E.N.E.S.R.)

المصدر: ISSN: 2155-5435.

مصطلحات موضوعية: Catalyzed ketone hydrogenation, Catalyzed transfer hydrogenation, Iridium, Bifunctional ligands, Asymmetric catalysis, Effect of strong base, [CHIM.COOR]Chemical Sciences/Coordination chemistry, [CHIM.CATA]Chemical Sciences/Catalysis, [CHIM.ORGA]Chemical Sciences/Organic chemistry

Relation: hal-01919616; https://hal.science/hal-01919616; https://hal.science/hal-01919616/document; https://hal.science/hal-01919616/file/349-10.1021.acscatal.5b00613-Accepted.pdf

الاتاحة: https://hal.science/hal-01919616
https://hal.science/hal-01919616/document
https://hal.science/hal-01919616/file/349-10.1021.acscatal.5b00613-Accepted.pdf
https://doi.org/10.1021/acscatal.5b00613

المؤلفون: Nicklaus, Celine M., Minnaard, Adriaan J., Feringa, Ben L., de Vries, Johannes G.

المصدر: Nicklaus , C M , Minnaard , A J , Feringa , B L & de Vries , J G 2013 , ' Synthesis of Renewable Fine-Chemical Building Blocks by Reductive Coupling between Furfural Derivatives and Terpenes ' , Chemsuschem , vol. 6 , no. 9 , pp. 1631-1635 . https://doi.org/10.1002/cssc.201300179

مصطلحات موضوعية: biomass, heterocycles, reductive couplings, ruthenium, terpenoids, ALDEHYDE OXIDATION LEVEL, ALLYL METAL REAGENTS, CATALYZED TRANSFER HYDROGENATION, FORMING TRANSFER HYDROGENATION, C-C BONDS, CARBONYL ALLYLATION, BETA,GAMMA-UNSATURATED KETONES, ALCOHOL, CROTYLATION, HYDROHYDROXYALKYLATION

وصف الملف: application/pdf

Relation: https://research.rug.nl/en/publications/6baa7818-4ad7-4d4b-8623-e47b0e14e2cc

الاتاحة: https://hdl.handle.net/11370/6baa7818-4ad7-4d4b-8623-e47b0e14e2cc
https://research.rug.nl/en/publications/6baa7818-4ad7-4d4b-8623-e47b0e14e2cc
https://doi.org/10.1002/cssc.201300179
https://pure.rug.nl/ws/files/6800350/2013ChemSusChemNicklaus.pdf
https://pure.rug.nl/ws/files/6800351/2013ChemSusChemNicklausSupp.pdf

المؤلفون: Vastila, P., Zaitsev, A. B., Wettergren, J., Privalov, Timofei, Adolfsson, H.

المصدر: Chemistry - A European Journal. 12(12):3218-3225

مصطلحات موضوعية: amino acids, amino alcohols, asymmetric catalysis, hydrogen transfer, ruthenium, asymmetric transfer-hydrogenation, alcohol)-catalyzed transfer hydrogenation, catalyzed transfer hydrogenation, ligand bifunctional catalysis, molecular-orbital methods, alpha-amino-acids, carbonyl-compounds, aerobic oxidation, transfer reduction, aromatic ketones

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-15630

المؤلفون: Eric Manoury, Gregori Ujaque, Eric Deydier, Joseph Hayes, Sandrine Vincendeau, Agustí Lledós, Rinaldo Poli, Raluca Malacea-Kabbara

المساهمون: Departament de Química [Barcelona] (UAB), Universitat Autònoma de Barcelona (UAB), Laboratoire de chimie de coordination (LCC), Institut National Polytechnique (Toulouse) (Toulouse INP), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie de Toulouse (ICT-FR 2599), Université Fédérale Toulouse Midi-Pyrénées-Université Fédérale Toulouse Midi-Pyrénées-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université Fédérale Toulouse Midi-Pyrénées-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche pour le Développement (IRD)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), Institut Universitaire de France (IUF), Ministère de l'Education nationale, de l’Enseignement supérieur et de la Recherche (M.E.N.E.S.R.), Institut de Chimie de Toulouse (ICT), Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Université de Toulouse (UT)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut National Polytechnique (Toulouse) (Toulouse INP), Université de Toulouse (UT)-Institut de Recherche pour le Développement (IRD)-Université Toulouse III - Paul Sabatier (UT3), Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS)

المصدر: ACS Catalysis
ACS Catalysis, American Chemical Society, 2015, 5 (7), pp.4368-4376. ⟨10.1021/acscatal.5b00613⟩
ACS Catalysis, 2015, 5 (7), pp.4368-4376. ⟨10.1021/acscatal.5b00613⟩

مصطلحات موضوعية: Effect of strong base, Ketone, Catalyzed transfer hydrogenation, F100, B200, Catalyzed ketone hydrogenation, Iridium, 010402 general chemistry, Photochemistry, 01 natural sciences, Heterolysis, Medicinal chemistry, Catalysis, Bifunctional ligands, chemistry.chemical_compound, Thioether, Asymmetric catalysis, [CHIM.COOR]Chemical Sciences/Coordination chemistry, Lewis acids and bases, chemistry.chemical_classification, [CHIM.ORGA]Chemical Sciences/Organic chemistry, 010405 organic chemistry, Hydride, [CHIM.CATA]Chemical Sciences/Catalysis, General Chemistry, 0104 chemical sciences, chemistry, Outer sphere electron transfer, Phosphine

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afa5e3baefed959a98b1f50782101516

المؤلفون: Samec, Joseph S. M., Backvall, Jan-E.

المصدر: Chemistry - A European Journal. 8(13):2955-2961

مصطلحات موضوعية: ruthenium catalyzed transfer hydrogenation imine propanol mechanism substituent effect

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-174625

المؤلفون: Celine M. Nicklaus, Adriaan J. Minnaard, Johannes G. de Vries, Ben L. Feringa

المساهمون: Stratingh Institute of Chemistry, Chemical Biology 2, Synthetic Organic Chemistry

المصدر: Chemsuschem, 6(9), 1631-1635. WILEY-V C H VERLAG GMBH

مصطلحات موضوعية: General Chemical Engineering, GAMMA-UNSATURATED KETONES, HYDROHYDROXYALKYLATION, Biomass, BETA, ALCOHOL, Chemistry Techniques, Synthetic, Furfural, BETA,GAMMA-UNSATURATED KETONES, CARBONYL ALLYLATION, Catalysis, Terpene, chemistry.chemical_compound, terpenoids, Environmental Chemistry, Organic chemistry, General Materials Science, reductive couplings, FORMING TRANSFER HYDROGENATION, Furaldehyde, ruthenium, GeneralLiterature_REFERENCE(e.g.,dictionaries,encyclopedias,glossaries), ALDEHYDE OXIDATION LEVEL, CATALYZED TRANSFER HYDROGENATION, heterocycles, biomass, business.industry, Terpenes, Green Chemistry Technology, CROTYLATION, Terpenoid, Renewable energy, ALLYL METAL REAGENTS, General Energy, chemistry, Yield (chemistry), C-C BONDS, ComputingMethodologies_DOCUMENTANDTEXTPROCESSING, Fine chemical, business, Oxidation-Reduction, Renewable resource

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::178a819c9438c32f773f30a52514172f
https://pubmed.ncbi.nlm.nih.gov/23857755

المؤلفون: Rüping, Magnus, Stoeckel, Mirjam, Sugiono, Erli, Theissmann, Thomas

المصدر: Tetrahedron : the international journal for the rapid publication of full original research papers and critical reviews in organic chemistry 66(33), 6565-6568 (2010). doi:10.1016/j.tet.2010.04.091

مصطلحات موضوعية: Flumequine, Levofloxacine, Bronsted acid, Asymmetric reduction, Organocatalysis, chiral phosphoric-acids, alpha-imino esters, enantioselective transfer hydrogenation, catalyzed transfer hydrogenation, optically-active ofloxacin, antibacterial activities, absolute-configuration, key intermediate, reaction cascade

جغرافية الموضوع: DE

Relation: info:eu-repo/semantics/altIdentifier/issn/0563-2064; info:eu-repo/semantics/altIdentifier/issn/0040-4020; info:eu-repo/semantics/altIdentifier/issn/1464-5416; info:eu-repo/semantics/altIdentifier/wos/WOS:000280902200033; https://publications.rwth-aachen.de/record/168706; https://publications.rwth-aachen.de/search?p=id:%22RWTH-CONV-046345%22

الاتاحة: https://publications.rwth-aachen.de/record/168706
https://publications.rwth-aachen.de/search?p=id:%22RWTH-CONV-046345%22

المؤلفون: Giri, Santanab, Wang, David Zhigang, Chattaraj, Pratim Kumar

المساهمون: Wang, DZ (reprint author), Peking Univ, Sch Chem Biol & Biotechnol, Shenzhen Grad Sch, Shenzhen 518055, Peoples R China., Peking Univ, Sch Chem Biol & Biotechnol, Shenzhen Grad Sch, Shenzhen 518055, Peoples R China., Indian Inst Technol, Dept Chem, Theoret Chem Lab, Kharagpur 721302, W Bengal, India.

المصدر: SCI

مصطلحات موضوعية: Electronic polarizability, Asymmetric hydrogenation, Linear free energy relationship, Enantiomeric excess, Rhodium phosphine complex, ALCOHOL)-CATALYZED TRANSFER HYDROGENATION, CHIRAL PHOSPHORUS LIGANDS, SOFT ACIDS, ENANTIOSELECTIVE HYDROGENATION, CHEMICAL-REACTIVITY, PROCHIRAL ENAMIDES, BOC-PYRROLIDINE, HSAB PRINCIPLE, BASES HSAB, RHODIUM

Relation: TETRAHEDRON.2010,66,(25),4560-4563.; 926665; http://hdl.handle.net/20.500.11897/243762; WOS:000278947100022

الاتاحة: https://hdl.handle.net/20.500.11897/243762
https://doi.org/10.1016/j.tet.2010.04.055

المؤلفون: Liu, Xiaochen

المصدر: Dissertations, Theses, and Capstone Projects

مصطلحات موضوعية: ring-opening of isoxazoles and isoxazolines, aged NMP, iron-catalyzed transfer hydrogenation, iodine-mediated C-N bond cross-coupling, formylation of amides, ICl-mediated functionalization of β-alkoxy alkynes, Organic Chemistry

وصف الملف: application/pdf

Relation: https://academicworks.cuny.edu/gc_etds/4319; https://academicworks.cuny.edu/context/gc_etds/article/5385/viewcontent/Xiaochen_Liu_Revised_Dissertation.pdf

الاتاحة: https://academicworks.cuny.edu/gc_etds/4319
https://academicworks.cuny.edu/context/gc_etds/article/5385/viewcontent/Xiaochen_Liu_Revised_Dissertation.pdf

المؤلفون: Bo-Bo Gou (5051204), Sen Yang (88300), Huai-Ri Sun (6083288), Qing-Song Jian (11796247), Atif Sharif (9083129), Ling Zhou (51948), Jie Chen (5892)

مصطلحات موضوعية: Biochemistry, Microbiology, Biotechnology, Computational Biology, Biological Sciences not elsewhere classified, newly developed protocol, catalyzed transfer hydrogenation, cyclization tandem reaction, cyclization reaction, stage modification, preliminary exploration, hydrogen source, good yields, enantioselective synthesis, effective sc, >‑ aminobenzaldehydes, >‑ aminoacetophenone

Relation: https://figshare.com/articles/journal_contribution/Scandium_Triflate_Catalyzed_Tandem_Transfer_Hydrogenation_and_Cyclization_Reaction_of_i_o_i_Aminobenzaldehydes_and_i_o_i_Aminoacetophenone_with_Alcohols/17128666

الاتاحة: https://doi.org/10.1021/acs.joc.1c01912.s001