المؤلفون: Triano Notario, Ángel

Thesis Advisors: Paco Sánchez, Pedro Antonio de

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: Xarxes en paral·lel, Redes en paralelo, Parallel-connected, Acoblaments creuats, Acoplamientos cruzados, Cross-couplings, Tecnologia d'ona acústica, Tecnología de onda acústica, acoustic wave Technology, Tecnologies

وصف الملف: application/pdf

URL الوصول: http://hdl.handle.net/10803/670935

المؤلفون: García Melchor, Maximiliano

المساهمون: University/Department: Universitat Autònoma de Barcelona. Departament de Química

Thesis Advisors: Ujaque Pérez, Gregori, Lledós, Agustí (Lledós i Falcó)

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: Palladium, cross-couplings, DFT calculations, Ciències Experimentals

وصف الملف: application/pdf

URL الوصول: http://hdl.handle.net/10803/96827

المؤلفون: Hu, Yuting, Li, Xiaohan, Jin, Gongzhen, Lipshutz, Bruce H

المصدر: ACS Catalysis. 13(5)

مصطلحات موضوعية: Nanotechnology, Bioengineering, nanoparticles, cross-couplings, micellar catalysis, chemistry in water, Pd catalysis, Inorganic Chemistry, Organic Chemistry, Chemical Engineering

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/4qw0p1vw
https://escholarship.org/content/qt4qw0p1vw/qt4qw0p1vw.pdf

المؤلفون: Adnan Ahmed, Irfan Mushtaq, Sampath Chinnam

المصدر: Future Journal of Pharmaceutical Sciences, Vol 9, Iss 1, Pp 1-22 (2023)

مصطلحات موضوعية: Suzuki–Miyaura, Metal catalyzed, Boron reagents, Organic synthesis, Cross-couplings, Therapeutics. Pharmacology, RM1-950, Pharmacy and materia medica, RS1-441

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2314-7253

URL الوصول: https://doaj.org/article/b20ca678e63244d88fe2408a4f7a763a

المؤلفون: Kjell Undheim

المصدر: Molecules, Vol 29, Iss 8, p 1815 (2024)

مصطلحات موضوعية: purine nucleobases, nucleosides and nucleotides, carbylations, oxidative metalations, cross-couplings, halogenations, Organic chemistry, QD241-441

Relation: https://www.mdpi.com/1420-3049/29/8/1815; https://doaj.org/toc/1420-3049; https://doaj.org/article/a5f327f83c5e41558bf0492b18e14432

الاتاحة: https://doi.org/10.3390/molecules29081815
https://doaj.org/article/a5f327f83c5e41558bf0492b18e14432

المؤلفون: Lima, Fabio

المساهمون: Ley, Steven Victor

مصطلحات موضوعية: 547, photoredox, catalysis, boronic acids, boronic esters, cross-couplings, synthetic methods, lewis base, flow, visible light, photochemistry

URL الوصول: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744718

المؤلفون: Delaunay, Oriane, Denicourt-Nowicki, Audrey, Roucoux, Alain

المساهمون: Institut des Sciences Chimiques de Rennes (ISCR), Université de Rennes (UR)-Institut National des Sciences Appliquées - Rennes (INSA Rennes), Institut National des Sciences Appliquées (INSA)-Institut National des Sciences Appliquées (INSA)-Ecole Nationale Supérieure de Chimie de Rennes (ENSCR)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Ministère de l’Enseignement Supérieur et de la Recherche (grant to O.D.)

المصدر: ISSN: 1867-3880.

مصطلحات موضوعية: N2O upgrading, photocatalysis, silver on titanium dioxide, homo- & cross- couplings, selective oxidation, [CHIM.ORGA]Chemical Sciences/Organic chemistry, [CHIM.CATA]Chemical Sciences/Catalysis

Relation: hal-04274219; https://hal.science/hal-04274219; https://hal.science/hal-04274219/document; https://hal.science/hal-04274219/file/accepted%20article-manuscript.pdf; CHEMRXIV: 10.26434/chemrxiv-2023-d2d3k

الاتاحة: https://hal.science/hal-04274219
https://hal.science/hal-04274219/document
https://hal.science/hal-04274219/file/accepted%20article-manuscript.pdf
https://doi.org/10.1002/cctc.202301269

المؤلفون: Zhen Fu, XiaoKun Wang, Xiaoyu Ren, Zhen Guo, Chengming Wang, Cong-Ying Zhou

مصطلحات موضوعية: Biochemistry, Medicine, Molecular Biology, Biotechnology, Immunology, Infectious Diseases, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, various functional groups, diaryl ether represents, construct diaryl ethers, cross coupling reaction, diaryl ethers, reaction proceeds, cross couplings, synthetic method, successfully applied, neutral conditions, high yields, diazo quinones, concise synthesis, catalyzed c, 7 inhibitor

Relation: https://figshare.com/articles/journal_contribution/Rhodium-Catalyzed_C_sp_sup_2_sup_O_Cross_Couplings_of_Diazo_Quinones_with_Phenols_to_Construct_Diaryl_Ethers/24917610

الاتاحة: https://doi.org/10.1021/acs.orglett.3c03969.s001
https://figshare.com/articles/journal_contribution/Rhodium-Catalyzed_C_sp_sup_2_sup_O_Cross_Couplings_of_Diazo_Quinones_with_Phenols_to_Construct_Diaryl_Ethers/24917610

المؤلفون: Sylwia Ostrowska, Lorenzo Palio, Agnieszka Czapik, Subhrajyoti Bhandary, Marcin Kwit, Kristof Van Hecke, Steven P. Nolan

المصدر: Catalysts; Volume 13; Issue 3; Pages: 559

مصطلحات موضوعية: palladacycle, weak base route, NHC, green solvent, C-C and C-heteroatom bonds formation, cross-couplings

وصف الملف: application/pdf

Relation: Catalysis in Organic and Polymer Chemistry; https://dx.doi.org/10.3390/catal13030559

الاتاحة: https://doi.org/10.3390/catal13030559

المؤلفون: Starnovskaya, E. S., Kopchuk, D. S., Shtaitz, Y. K., Savchuk, M. I., Nikonov, I. L., Egorov, I. N., Zyryanov, G. V., Rusinov, V. L., Chupakhin, O. N.

المصدر: J Fluoresc ; Journal of Fluorescence

مصطلحات موضوعية: 1,2,4-TRIAZINES, 1,3-DI(2-PYRIDYL)BENZENES, AZA-DIELS–ALDER REACTION, CROSS-COUPLING, FLUORESCENCE, BENZENE, CHEMICAL REACTIONS, 1,2,4-TRIAZINE, 1,3-DI(2-PYRIDYL)BENZENE, CROSS-COUPLINGS, DIELS-ALDER REACTION, FUNCTIONALIZED, PHOTOPHYSICAL STUDIES, PYRIDYL, STILLE CROSS-COUPLING, SYNTHETIC APPROACH, ARTICLE, DIELS ALDER REACTION, STILLE REACTION, SYNTHESIS

وصف الملف: application/pdf

Relation: info:eu-repo/grantAgreement/RSF//19-73-10144; Asymmetrically Functionalized 1,3-Di(2-pyridyl)benzenes: Synthesis and Photophysical Studies / E. S. Starnovskaya, D. S. Kopchuk, Y. K. Shtaitz et al. // Journal of Fluorescence. — 2022. — Vol. 32. — Iss. 1. — P. 125-133.; All Open Access, Bronze; http://elar.urfu.ru/handle/10995/111952; 85116515008; 000705724700001

الاتاحة: http://elar.urfu.ru/handle/10995/111952
https://doi.org/10.1007/s10895-021-02759-4

المؤلفون: Schmidt, Sandy

المصدر: Schmidt , S 2022 , ' Photoexcited enzymes for asymmetric Csp3-Csp3 cross-electrophile couplings ' , Angewandte Chemie International Edition , vol. 61 , no. 52 , e202214313 . https://doi.org/10.1002/anie.202214313

مصطلحات موضوعية: abiological transformations, biocatalysis, cross couplings, ene-reductases, photocatalysis

وصف الملف: application/pdf

الاتاحة: https://hdl.handle.net/11370/7901fdf7-f392-4b58-8946-79f7edaf905f
https://research.rug.nl/en/publications/7901fdf7-f392-4b58-8946-79f7edaf905f
https://doi.org/10.1002/anie.202214313
https://pure.rug.nl/ws/files/573891152/Angew_Chem_Int_Ed_2022_Schmidt_Photoexcited_Enzymes_for_Asymmetric_Csp3_Csp3_Cross_Electrophile_Couplings.pdf

المؤلفون: Горбійчук, М. І., Лазорів, Н. Т., Когутяк, М. І., Лазорів, А. М.

مصطلحات موضوعية: муфельна піч, перехресні зв’язки, компенсатор, передавальні функції, декомпозиція, z-перетворення, оцінка, точність, muffle furnace, cross couplings, compensator, transfer functions, decomposition, z-transform, evaluation, accuracy

Relation: Дослідження динамічних властивостей компенсатора перехресних зв'язків автономної системи керування / М. І. Горбійчук, Н. Т. Лазорів, М. І. Когутяк, А. М. Лазорів // Методи та прилади контролю якості. - 2022. - № 2. - С. 74-88.; http://elar.nung.edu.ua/handle/123456789/9263

الاتاحة: http://elar.nung.edu.ua/handle/123456789/9263

المؤلفون: Handa, Sachin, Slack, Eric D, Lipshutz, Bruce H

المصدر: Angewandte Chemie International Edition. 54(41)

مصطلحات موضوعية: Bioengineering, Nanotechnology, Boronic Acids, Bromides, Catalysis, Green Chemistry Technology, Hydrocarbons, Aromatic, Metal Nanoparticles, Micelles, Models, Molecular, Nickel, Water, cross-couplings, green chemistry, micelles, nanoparticles, nickel, Chemical Sciences, Organic Chemistry, Chemical sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/8441h375
https://escholarship.org/content/qt8441h375/qt8441h375.pdf

المؤلفون: Mazars, François, Etse, Koffi Senam, Zaragoza, Guillermo, Delaude, Lionel

المصدر: Journal of Organometallic Chemistry, 1003, 122928 (2023-12-15)

مصطلحات موضوعية: Alkaloids, Carbene ligands, Cross-coupling, Green chemistry, Hirshfeld surface, Aryl bromides, Arylation reactions, Catalyst precursors, Cross-couplings, Electron-withdrawing substituents, Green-chemistry, Hirshfeld surfaces, N-heterocyclic carbene ligands, ]+ catalyst, Biochemistry, Physical and Theoretical Chemistry, Organic Chemistry, Inorganic Chemistry, Materials Chemistry, Physical, chemical, mathematical & earth Sciences, Chemistry, Physique, chimie, mathématiques & sciences de la terre, Chimie

Relation: https://api.elsevier.com/content/article/PII:S0022328X23003169?httpAccept=text/xml; urn:issn:0022-328X

URL الوصول: https://orbi.uliege.be/handle/2268/309258

المؤلفون: Hänni, Kevin D.

المساهمون: Leigh, David A.

مصطلحات موضوعية: 541.39, transition metal-catalysed reactions, active-metal template reactions, interlocked architectures, Heck cross-couplings

URL الوصول: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.562479

المؤلفون: Martín García, María Trinidad, Marín Gómez, Mario, Maya Díaz, Celia María, Prieto Cárdenas, María Auxiliadora, Nicasio Jaramillo, María del Carmen

المساهمون: Universidad de Sevilla. Departamento de Química Inorgánica, Agencia Estatal de Investigación. España CTQ2017-82893- C2-2-R

مصطلحات موضوعية: C−S bond formation, Dual chemoselectivity, Ni catalysis, Phosphine complexes, Andem cross-couplings

Relation: Chemistry - A European Journal, 27 (48), 12320-12326.; CTQ2017-82893- C2-2-R; US126226; https://doi.org/10.1002/chem.202101906; https://idus.us.es/handle//11441/128218

الاتاحة: https://idus.us.es/handle//11441/128218

المؤلفون: Martín, M. Trinidad, Marín, Mario, Maya, Celia, Prieto Cárdenas, María Auxiliadora, Nicasio Jaramillo, María Carmen

مصطلحات موضوعية: C-S bond formation, Ni catalysis, Phosphine complexes, Dual chemoselectivity, Tandem cross-couplings, 23 Química

Relation: Martín, M. T., Marín, M., Maya, C., Prieto, A., & Nicasio, M. C. (2021). Ni(II) Precatalysts Enable Thioetherification of (Hetero)Aryl Halides and Tosylates and Tandem C−S/C−N Couplings. Chemistry – A European Journal, 27(48), 12320–12326. https://doi.org/10.1002/chem.202101906; http://hdl.handle.net/10272/20060

الاتاحة: http://hdl.handle.net/10272/20060
https://doi.org/10.1002/chem.202101906

المؤلفون: Mkrtchyan, Satenik, Jakubczyk, Michal, Lanka, Suneel, Pittelkow, Michael, Iaroshenko, Viktor O.

المساهمون: Helsinki Institute of Sustainability Science (HELSUS), Department of Chemistry

مصطلحات موضوعية: fluorine, amides, copper, catalysis, C-C-coupling, boronic acids, aryl trialkoxysilanes, dimethyl-aryl-sulfonium salts, PHOTOREDOX CATALYSIS, ARYLBORONATE ESTERS, CROSS-COUPLINGS, BOND FORMATION, AMINODIFLUOROALKYLATION, TRANSFORMATION, RECOGNITION, MECHANISM, ACCESS, Chemical sciences

وصف الملف: application/pdf

Relation: This research was supported by a grant from National Science Centre (NSC) Poland within the framework of European Union?s Horizon 2020 research and innovation program under the Marie Sk?odowska-Curie grant agreement No. 665778 (POLONEZ 2 grant, Nr. 2016/21/P/ST5/00630) obtained by Satenik Mkrtchyan. This research project was also supported by a grant from National Science Centre (NSC) Poland, the SONATA 10 (Nr. 2015/19/D/ST5/02774) obtained by Viktor Iaroshenko. Viktor Iaroshenko also acknowledges the funding for his Visiting Professorship from the University of Salerno. Michael Pittelkow appreciates the support from the Danish Council for Independent Research (DFF 4181-00206 and 9040-00265) and from the University of Copenhagen. Funding: This research was supported by a grant from National Science Centre (NSC) Poland within the framework of European Union’s Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant agreement No. 665778 (POLONEZ 2 grant, Nr. 2016/21/P/ST5/00630) obtained by Satenik Mkrtchyan. This research project was also supported by a grant from National Science Centre (NSC) Poland, the SONATA 10 (Nr. 2015/19/D/ST5/02774) obtained by Viktor Iaroshenko. Viktor Iaroshenko also acknowledges the funding for his Visiting Professorship from the University of Salerno. Michael Pittelkow appreciates the support from the Danish Council for Independent Research (DFF 4181-00206 and 9040-00265) and from the University of Copenhagen.; Mkrtchyan , S , Jakubczyk , M , Lanka , S , Pittelkow , M & Iaroshenko , V O 2021 , ' Cu-Catalyzed Arylation of Bromo-Difluoro-Acetamides by Aryl Boronic Acids, Aryl Trialkoxysilanes and Dimethyl-Aryl-Sulfonium Salts : New Entries to Aromatic Amides ' , Molecules , vol. 26 , no. 10 , 2957 . https://doi.org/10.3390/molecules26102957; ORCID: /0000-0002-5647-5326/work/95673805; http://hdl.handle.net/10138/331474; 77064d49-cde8-4d5d-a2b1-9b10b349e570; 000655048400001

الاتاحة: http://hdl.handle.net/10138/331474

المؤلفون: Lucius Schmid (5884199), Christoph Kerzig (6251597), Alessandro Prescimone (1446697), Oliver S. Wenger (1282311)

مصطلحات موضوعية: Biochemistry, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, reductive photoredox catalysis, α- diimine ligands, excited-state energies, 3 MLCT energies, photoisomerization reactions, metal-based t 2 g, 3 groups, pinacol couplings, luminescence quantum yields, future applications, 2.50 eV, nonradiative excited-state relaxati., photoactive metal-to-ligand charge-., photoactive coordination compounds, α- diimine, MLCT lifetimes, excited-state redox power, isocyanoborato complexes, higher-lying metal-centered states, CN, triplet energy, photorobust compounds, Energy Transfer, energy conversion, energy transfer catalysis, nickel-catalyzed cross-couplings

Relation: https://figshare.com/articles/journal_contribution/Photostable_Ruthenium_II_Isocyanoborato_Luminophores_and_Their_Use_in_Energy_Transfer_and_Photoredox_Catalysis/14593759

الاتاحة: https://doi.org/10.1021/jacsau.1c00137.s001

المؤلفون: Jingjun Huang (5353856), Matthew Isaac (10692487), Ryan Watt (10692490), Joseph Becica (4338466), Emma Dennis (10692493), Makhsud I. Saidaminov (1371087), William A. Sabbers (5492600), David C. Leitch (1837264)

مصطلحات موضوعية: Biophysics, Medicine, Molecular Biology, Physiology, Biotechnology, Sociology, Space Science, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, maleic anhydride, high-throughput experimentation, phosphine precatalysts, DMP, preparative-scale cross-couplings, microscale reaction screens, Precatalyst Formation, DAB, Preparative-Scale Synthesis, plate-based reaction arrays, reaction screening, Pd loadings, diazabutadiene ligand, bidentate phosphines, large-cone-angle biarylphosphines, Pd source, chelating N, room temperature, catalyst preparation

Relation: https://figshare.com/articles/journal_contribution/_sup_DMP_sup_DAB_Pd_MAH_A_Versatile_Pd_0_Source_for_Precatalyst_Formation_Reaction_Screening_and_Preparative-Scale_Synthesis/14475889

الاتاحة: https://doi.org/10.1021/acscatal.1c00288.s001