المؤلفون: Ubasart Clarà, Ernest

المساهمون: University/Department: Universitat de Girona. Departament de Química, University/Department: Universitat de Girona. Institut de Química Computacional i Catàlisi

مرشدي الرسالة: ernest.ubasart@gmail.com, Ribas Salamaña, Xavi

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: Funcionalització regioselectiva de C60, Funcionalización regioselectiva de C60, Regioselective functionalization of C60, Estretègia de màscara supramolecular, Estretgia de máscara supramolecular, Supramolecular mask strategy, Derivats de ful·lerè, Derivados de fullereno, Fullerene derivatives, Química amfitrió-convidat, Química anfitrión-invitado, Host-guest chemistry, Purificació supramolecular de C84, Purificación supramolecular de C84, Supramolecular purification of C84, Estabilització supramolecular de nanopartícules metàl·liques, Estabilitzación supramolecular de nanopartículas metálicas, Supramolecular stabilization of metallic nanoparticles, Nanocàpsules supramoleculars prismàtiques tetragonals autoensamblades, Nanocápsulas supramoleculares prismáticas tetragonales autoensambladas, Self-assembled tetragonal prismatic supramolecular nanocapsules

وصف الملف: application/pdf

الوصول الحر: http://hdl.handle.net/10803/687537Test

المؤلفون: Guo, Mengzhe, Ede, James, Sayes, Christie, Shatkin, Jo, Stark, Nicole, Hsieh, You-Lo

المصدر: Nanomaterials. 14(5)

مصطلحات موضوعية: C2, C3 regioselective, TEMPO, cellulose nanofibril, dissolving pulp, periodate–chlorite oxidation

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/2j65n8x2Test

المؤلفون: Llinàs Riera, Maria del Carme

المساهمون: University/Department: Universitat Ramon Llull. IQS SE - Química Orgànica i Farmacèutica (2015 - )

مرشدي الرسالة: Sánchez García, David

المصدر: TDX (Tesis Doctorals en Xarxa)

مصطلحات موضوعية: Mesoporous silica nanoparticles, Regioselective bifunctionalization, Drug delivery, Anion Sensing, Nanotechnology, Biomedicine, Ciències

وصف الملف: application/pdf

الوصول الحر: http://hdl.handle.net/10803/369849Test

المؤلفون: Severin Mairinger, Matthias Jackwerth, Ondřej Soukup, Matthias Blaickner, Clemens Decristoforo, Lukas Nics, Jens Pahnke, Marcus Hacker, Markus Zeitlinger, Oliver Langer

المصدر: EJNMMI Radiopharmacy and Chemistry, Vol 9, Iss 1, Pp 1-13 (2024)

مصطلحات موضوعية: 6-Bromo-7-[11C]methylpurine, Investigational medicinal product dossier, Multidrug resistance-associated protein 1, PET, Regioselective N‑alkylation, Medical physics. Medical radiology. Nuclear medicine, R895-920, Therapeutics. Pharmacology, RM1-950

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2365-421XTest

الوصول الحر: https://doaj.org/article/c48cb573bf5448948f7a081af7f99130Test

المؤلفون: Yong‐Ju Kwon, Ye‐Jin Kong, Min‐Jung Lee, Eun‐Hye Lim, Jaesung Kwak, Won‐Suk Kim

المصدر: Advanced Science, Vol 11, Iss 17, Pp n/a-n/a (2024)

مصطلحات موضوعية: amidobenzyne precursors, aryne, bimetallic cross‐coupling, oxy‐argentation, regioselective arylation, Science

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/2198-3844Test

الوصول الحر: https://doaj.org/article/82fc95ca423141978606177786ff7c28Test

المؤلفون: Mark Reihill, Hanyue Ma, Dennis Bengtsson, Stefan Oscarson

المصدر: Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 173-180 (2024)

مصطلحات موضوعية: regioselective sulfation, thioglycoside donors, thomsen–friedenreich antigen, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1860-5397Test

الوصول الحر: https://doaj.org/article/abf7d1f501254d23a0fdbfa06f966809Test

المؤلفون: Matchavariani, David, Popek, Lucas, Cabrera-Trujillo, Jorge, Nguyen, Thi, Mo, Blanchard, Nicolas, Miqueu, Karinne, Cahard, Dominique, Bizet, Vincent

المساهمون: Laboratoire d'innovation moléculaire et applications (LIMA), Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Institut des sciences analytiques et de physico-chimie pour l'environnement et les materiaux (IPREM), Université de Pau et des Pays de l'Adour (UPPA)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Chimie Organique et Bioorganique : Réactivité et Analyse (COBRA), Institut de Chimie Organique Fine (IRCOF), Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU)-Institut national des sciences appliquées Rouen Normandie (INSA Rouen Normandie), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)-Université de Rouen Normandie (UNIROUEN), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)-Institut Normand de Chimie Moléculaire Médicinale et Macromoléculaire (INC3M), Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Normandie Université (NU)-École Nationale Supérieure d'Ingénieurs de Caen (ENSICAEN), Normandie Université (NU)-Université Le Havre Normandie (ULH), Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Institut national des sciences appliquées Rouen Normandie (INSA Rouen Normandie), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université de Caen Normandie (UNICAEN), Normandie Université (NU)-École Nationale Supérieure d'Ingénieurs de Caen (ENSICAEN), Normandie Université (NU)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), ANR-21-CE07-0042,SulFive,Assurer un brillant avenir à la chimie émergente du motif SF5(2021)

المصدر: ISSN: 1615-4150.

مصطلحات موضوعية: pentafluorosulfanyl halogenation SF 5 -alkyne regioselective and stereodivergent DFT, pentafluorosulfanyl, halogenation, SF 5 -alkyne, regioselective and stereodivergent, DFT, [CHIM.MATE]Chemical Sciences/Material chemistry, [CHIM.ANAL]Chemical Sciences/Analytical chemistry, [CHIM.POLY]Chemical Sciences/Polymers, [CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistry

العلاقة: hal-04606248; https://univ-pau.hal.science/hal-04606248Test; https://univ-pau.hal.science/hal-04606248/documentTest; https://univ-pau.hal.science/hal-04606248/file/Adv%20Synth%20Catal%20-%202024%20-%20Matchavariani%20-%20Ambiphilic%20Reactivity%20of%20SF5%E2%80%90Alkynes%20Applied%20to%20Regioselective%20and%20Stereodivergent-3.pdfTest

الإتاحة: https://doi.org/10.1002/adsc.202400446Test
https://univ-pau.hal.science/hal-04606248Test
https://univ-pau.hal.science/hal-04606248/documentTest
https://univ-pau.hal.science/hal-04606248/file/Adv%20Synth%20Catal%20-%202024%20-%20Matchavariani%20-%20Ambiphilic%20Reactivity%20of%20SF5%E2%80%90Alkynes%20Applied%20to%20Regioselective%20and%20Stereodivergent-3.pdfTest

المؤلفون: Helian Li, Yongxin Zhang, Xiuyuan Zou, Xiaoxiao Yang, Pan Zhou, Xinyue Ma, Shuaiqi Lu, Qing Sun, Chao Shu

مصطلحات موضوعية: Biophysics, Biochemistry, Genetics, Molecular Biology, Biotechnology, Evolutionary Biology, Developmental Biology, Infectious Diseases, Chemical Sciences not elsewhere classified, operationally simple conditions, multicomponent fragment coupling, diverse downstream transformations, broad substrate scope, attracted significant attention, extremely challenging due, strategy provides access, photoinduced regioselective sulfonylsulfination, alkenes regioselective 1, otherwise challenging, synthetic potential, sulfur atom, stage functionalization, sequential sulfonyl, reactions proceed, obtained products, inherent characteristics, high regio, group tolerance, complex molecules

العلاقة: https://figshare.com/articles/journal_contribution/Photoinduced_Regioselective_Sulfonylsulfination_of_Alkenes/25259384Test

الإتاحة: https://doi.org/10.1021/acscatal.4c00049.s001Test
https://figshare.com/articles/journal_contribution/Photoinduced_Regioselective_Sulfonylsulfination_of_Alkenes/25259384Test

المؤلفون: Young Hyun Hong, Madhuri Nilajakar, Yong-Min Lee, Wonwoo Nam, Shunichi Fukuzumi

مصطلحات موضوعية: Biochemistry, Medicine, Microbiology, Cell Biology, Geology, Marine Biology, Cancer, Inorganic Chemistry, Infectious Diseases, Computational Biology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, two liquid membranes, despite extensive efforts, four protons taken, >- benzoquinone derivatives, 2 +, h using water, psii model ), hydroquinone derivatives, four electrons, molecular model, turnover number, regioselective reduction, regioselective formation, reduce co, q ), psii models, psi model, proton sources

العلاقة: https://figshare.com/articles/journal_contribution/Artificial_Photosynthesis_for_Regioselective_Reduction_of_NAD_P_sup_sup_to_NAD_P_H_Using_Water_as_an_Electron_and_Proton_Source/25216250Test

الإتاحة: https://doi.org/10.1021/jacs.3c10369.s001Test
https://figshare.com/articles/journal_contribution/Artificial_Photosynthesis_for_Regioselective_Reduction_of_NAD_P_sup_sup_to_NAD_P_H_Using_Water_as_an_Electron_and_Proton_Source/25216250Test

المؤلفون: Ruiqin Zhang, Renchao Ma, Rener Chen, Lei Wang, Yongmin Ma

مصطلحات موضوعية: Biochemistry, Medicine, Pharmacology, Biotechnology, Ecology, Sociology, Mental Health, Infectious Diseases, Plant Biology, Chemical Sciences not elsewhere classified, free regioselective c, 3 , regioselective c, turbomycin b, transition metals, strong base, reaction avoids, protocol provides, favorable route, efficient transition

العلاقة: https://figshare.com/articles/journal_contribution/Regioselective_C_sub_3_sub_Alkylation_of_Indoles_for_the_Synthesis_of_Bis_indolyl_methanes_and_3_Styryl_Indoles/24991019Test

الإتاحة: https://doi.org/10.1021/acs.joc.3c02551.s001Test
https://figshare.com/articles/journal_contribution/Regioselective_C_sub_3_sub_Alkylation_of_Indoles_for_the_Synthesis_of_Bis_indolyl_methanes_and_3_Styryl_Indoles/24991019Test