المؤلفون: Avital Shifrovitch, Moran Madmon, Tamar Shamai Yamin, Avi Weissberg

المصدر: Organics, Vol 5, Iss 4, Pp 614-622 (2024)

مصطلحات موضوعية: free chlorine, aqueous media, derivatization, electrophilic aromatic substitution, LC-ESI-MS/MS, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2673-401X/5/4/32; https://doaj.org/toc/2673-401X

URL الوصول: https://doaj.org/article/e298fb2aac98403dbf7c0a2ca80711d1

المؤلفون: Roman A. Irgashev, Nikita A. Kazin

المصدر: Organics, Vol 5, Iss 4, Pp 507-519 (2024)

مصطلحات موضوعية: 3-nitrothiophenes, leaving nitro group, thiols, thieno[3,2-b]thiohenes, nucleophilic aromatic substitution, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://www.mdpi.com/2673-401X/5/4/27; https://doaj.org/toc/2673-401X

URL الوصول: https://doaj.org/article/3568dc7eeba5466ea06b6b22ac946e9b

المؤلفون: Susila Thapa, Jeanne L. Bolliger

المصدر: Molbank, Vol 2024, Iss 4, p M1942 (2024)

مصطلحات موضوعية: heterocycles, quinazoline, quinazolin-4(3H)-one, nucleophilic aromatic substitution, reduction, Inorganic chemistry, QD146-197

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-8599/2024/4/M1942; https://doaj.org/toc/1422-8599

URL الوصول: https://doaj.org/article/b65954bbedc145308b6055e5dcecaa61

المؤلفون: Vitor A. S. Almodovar, Augusto C. Tomé

المصدر: Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 1933-1939 (2024)

مصطلحات موضوعية: diketopyrrolopyrrole, fluorescent dye, nucleophilic aromatic substitution, phenol, thiol, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1860-5397

URL الوصول: https://doaj.org/article/162de7e5cd5143ba8ad48285be7fd22c

المؤلفون: Buchanan, Adam

مصطلحات موضوعية: Chemistry, Fluorine atoms, fluorine atom substitution, nucleophilic aromatic substitution (SNAr), ball milling synthesis, mechanochemistry ball milling, Truce-Smiles Rearrangement, Fluoroarenes, Neglected diseases, Neglected Diseases initiative, Chagas disease drug discovery, African Sleeping SicknessTrypanosoma brucei, leishmaniasis Visceral leishmaniasis

URL الوصول: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.885954

المؤلفون: Fatemeh Salehzadeh, Maryam Esmkhani, Milad Noori, Shahrzad Javanshir, Aida Iraji, Mohammad Mahdavi

المصدر: Frontiers in Chemistry, Vol 12 (2024)

مصطلحات موضوعية: Csp 2–Csp 2 cross-coupling reactions, microwave-assisted organic synthesis, nucleophilic aromatic substitution, antimicrobial, natural product cephalandole A, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fchem.2024.1472342/full; https://doaj.org/toc/2296-2646

URL الوصول: https://doaj.org/article/a94df24d1e9c47bea3c51083cf65f74e

المؤلفون: Hongfei Sun, Xianying Wu, Bin Yao, Guowang Li, Ning Qi, Lei Shi

المصدر: Arabian Journal of Chemistry, Vol 17, Iss 10, Pp 105987- (2024)

مصطلحات موضوعية: Ladder-type, Covalent organic frameworks, Topology design, Condensation reaction, Nucleophilic aromatic substitution reaction, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S1878535224003897; https://doaj.org/toc/1878-5352

URL الوصول: https://doaj.org/article/4c8c241817c2401188e3b8b118aaf7fe

المؤلفون: Victoria M. Alpatova, Evgeny G. Rys, Elena G. Kononova, Valentina A. Ol'shevskaya

المصدر: Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 767-776 (2024)

مصطلحات موضوعية: bioconjugation, carboranes, fluorine, porphyrin, snar aromatic substitution, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1860-5397

URL الوصول: https://doaj.org/article/cb0f745a2a554eafa763f16ae9429298

المؤلفون: Nitu, Cristina, van der Wal, Jacob Jan, Kaul, Nidhi, Steen, Jorn D., Hammarström, Leif, 1964, Fagnoni, Maurizio, Crespi, Stefano

المصدر: European Journal of Organic Chemistry. 27(1)

مصطلحات موضوعية: Aromatic substitution, Substituent effects, Computational chemistry, Conical intersections, Photochemistry

وصف الملف: electronic

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-528416
https://doi.org/10.1002/ejoc.202300461
https://uu.diva-portal.org/smash/get/diva2:1861362/FULLTEXT01.pdf

المؤلفون: Almodôvar, Vítor Alexandre da Silva

مصطلحات موضوعية: Diketopyrrolopyrroles, Suzuki-Miyaura, Nucleophilic aromatic substitution, Photophysical properties, Biological applications, Sensors

وصف الملف: application/pdf

الاتاحة: http://hdl.handle.net/10773/40202

المؤلفون: Paul R. Palme, Richard Goddard, Peter Imming, Rüdiger W. Seidel

المصدر: Molbank, Vol 2024, Iss 1, p M1795 (2024)

مصطلحات موضوعية: thiomorpholine, nucleophilic aromatic substitution, crystal structure, Hirshfeld surface analysis, DFT calculation, hydrogen bonding, Inorganic chemistry, QD146-197

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-8599/2024/1/M1795; https://doaj.org/toc/1422-8599

URL الوصول: https://doaj.org/article/494cfc975dc34af2ab40cf9e7827c266

المؤلفون: Chadron M. Friesen, Nathan J. Weeks, Scott T. Iacono

المصدر: Molbank, Vol 2024, Iss 1, p M1777 (2024)

مصطلحات موضوعية: organo-fluorine, pyridine, pentafluoropyridine, 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), nucleophilic aromatic substitution, Inorganic chemistry, QD146-197

وصف الملف: electronic resource

Relation: https://www.mdpi.com/1422-8599/2024/1/M1777; https://doaj.org/toc/1422-8599

URL الوصول: https://doaj.org/article/3a583dc954cb4d2383edd8d43c127f2d

المؤلفون: Andrea Salazar, Felipe Otálvaro

المصدر: Results in Chemistry, Vol 7, Iss , Pp 101404- (2024)

مصطلحات موضوعية: Phenylphenalenones, Buchwald aromatic substitution, Microwave-assisted synthesis, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2211715624001000; https://doaj.org/toc/2211-7156

URL الوصول: https://doaj.org/article/e9d82342fe5d4b339ff7b506226ad750

المؤلفون: Cerqueira, Ana F. R., Pinto, Ana Lúcia, Malta, Gabriela, Neves, Maria G. P. M. S., Parola, A. Jorge, Tomé, Augusto C.

المساهمون: LAQV@REQUIMTE, DQ - Departamento de Química

مصطلحات موضوعية: dye-sensitized solar cells, nucleophilic aromatic substitution, porphyrins, power conversion efficiency, thiols, Catalysis, Molecular Biology, Spectroscopy, Computer Science Applications, Physical and Theoretical Chemistry, Organic Chemistry, Inorganic Chemistry, SDG 7 - Affordable and Clean Energy

Relation: PURE: 99833489; Scopus: 85195847854; WOS: 001246547700001; PubMed: 38892167; PubMedCentral: PMC11172761; http://hdl.handle.net/10362/172412; https://doi.org/10.3390/ijms25115979

الاتاحة: http://hdl.handle.net/10362/172412
https://doi.org/10.3390/ijms25115979

المؤلفون: Samvel N. Sirakanyan, Domenico Spinelli, Edoardo Jun Mattioli, Matteo Calvaresi, Athina Geronikaki, Victor G. Kartsev, Elmira K. Hakobyan, Hasmik A. Yegoryan, Hasmik V. Jughetsyan, Mariam E. Manukyan, Anush A. Hovakimyan

المصدر: International Journal of Molecular Sciences ; Volume 25 ; Issue 22 ; Pages: 11977

مصطلحات موضوعية: 2,7-naphthyridine derivatives, nucleophilic aromatic substitution (S N Ar), rearrangement reactions, Smiles rearrangement, NMR, Schiff bases, ESP charges

جغرافية الموضوع: agris

وصف الملف: application/pdf

Relation: Molecular Nanoscience; https://dx.doi.org/10.3390/ijms252211977

الاتاحة: https://doi.org/10.3390/ijms252211977

المؤلفون: Bourbon, Paul, Vitse, Kassandra, Martin-Mingot, Agnès, Geindre, Hugo, Guégan, Frédéric, Michelet, Bastien, Thibaudeau, Sébastien

المساهمون: Institut de chimie des milieux et matériaux de Poitiers UMR 7285 (IC2MP Poitiers ), Université de Poitiers = University of Poitiers (UP)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Université de Poitiers - Faculté de Sciences fondamentales et appliquées, Université de Poitiers = University of Poitiers (UP)

المصدر: ISSN: 2041-1723.

مصطلحات موضوعية: Superacid, Electrophilic aromatic substitution, Methylation, Superelectrophile, [CHIM.ORGA]Chemical Sciences/Organic chemistry

الاتاحة: https://hal.science/hal-04680872
https://hal.science/hal-04680872v1/document
https://hal.science/hal-04680872v1/file/2024%20-%20Leveraging%20long-lived%20arenium%20ions%20in%20superacid%20for%20meta-selective%20methylation.pdf
https://doi.org/10.1038/s41467-024-49421-8

المؤلفون: Paoli-Lombardo, Romain, Primas, Nicolas, Bourgeade-Delmas, Sandra, Sournia-Saquet, Alix, Castera-Ducros, Caroline, Jacquet, Inès, Verhaeghe, Pierre, Rathelot, Pascal, Vanelle, Patrice

المساهمون: Institut de Chimie Radicalaire (ICR), Aix Marseille Université (AMU)-Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS), Pharmacochimie et Biologie pour le Développement (PHARMA-DEV), Institut de Recherche pour le Développement (IRD)-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), Laboratoire de chimie de coordination (LCC), Institut de Chimie de Toulouse (ICT), Université de Toulouse (UT)-Centre National de la Recherche Scientifique (CNRS), Hôpital de la Conception CHU - APHM (LA CONCEPTION), Département de pharmacochimie moléculaire (DPM), Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Université Grenoble Alpes (UGA)

المصدر: ISSN: 0039-7881 ; EISSN: 1437-210X.

مصطلحات موضوعية: Nitroaromatic, imidazo[1, 2-a]pyridine, kinetoplastids, nucleophilic aromatic substitution, palladium-catalyzed cross-coupling reaction, microwave irradiation, [CHIM]Chemical Sciences

Relation: IRD: fdi:010091877; WOS: 001318785900001

الاتاحة: https://amu.hal.science/hal-04534726
https://amu.hal.science/hal-04534726v1/document
https://amu.hal.science/hal-04534726v1/file/Paoli.pdf
https://doi.org/10.1055/a-2232-8113

المؤلفون: Nikitin, Sergei, Diness, Frederik

المصدر: Nikitin , S & Diness , F 2024 , ' Tuning Green Explosives through S N Ar Chemistry ' , Chemistry - An Asian Journal , vol. 19 , no. 13 , e202400212 . https://doi.org/10.1002/asia.202400212

مصطلحات موضوعية: azides, benzofuroxans, fluorine chemisty, high-energy materials, nucleophilic aromatic substitution

وصف الملف: application/pdf

الاتاحة: https://forskning.ruc.dk/da/publications/5b18792c-a9ac-4599-a696-8519c9b42b54
https://doi.org/10.1002/asia.202400212
https://hdl.handle.net/1800/5b18792c-a9ac-4599-a696-8519c9b42b54
https://rucforsk.ruc.dk/ws/files/104221333/Chemistry_An_Asian_Journal_-_2024_-_Nikitin_-_Tuning_Green_Explosives_through_SNAr_Chemistry.pdf

المؤلفون: Chander Shekhar, Gedu Satyanarayana

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Genetics, Molecular Biology, Biotechnology, Evolutionary Biology, Infectious Diseases, Computational Biology, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, two indole molecules, substituted benzo [<, second indole molecule, promoted domino pathway, promoted domino access, pot regioselective construction, photophysical properties study, mechanistic studies suggested, dual aromatic substitution, free reaction conditions, cinnamate ester followed, >] carbazoles herein, >] carbazoles, cinnamate esters, protecting group, ortho <, intramolecular cyclization, initial formation, free indoles

Relation: https://figshare.com/articles/journal_contribution/Acid-Promoted_Domino_Access_to_Substituted_Benzo_i_b_i_carbazoles/25282436

الاتاحة: https://doi.org/10.1021/acs.joc.3c02483.s001
https://figshare.com/articles/journal_contribution/Acid-Promoted_Domino_Access_to_Substituted_Benzo_i_b_i_carbazoles/25282436

المؤلفون: Diane N. Le, Mikhail Reibarkh, Daniel A. DiRocco, Yining Ji

مصطلحات موضوعية: Biochemistry, Medicine, Genetics, Molecular Biology, Biotechnology, Developmental Biology, Infectious Diseases, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, nucleophilic aromatic substitution, classical transformation suffered, overcoming product inhibition, n , product inhibition, synthetic challenge, related analogues, mechanistic studies, judicious choice, achieve reactivity

Relation: https://figshare.com/articles/journal_contribution/Overcoming_Product_Inhibition_in_a_Nucleophilic_Aromatic_Substitution_Reaction/25015827

الاتاحة: https://doi.org/10.1021/acs.orglett.3c03881.s001
https://figshare.com/articles/journal_contribution/Overcoming_Product_Inhibition_in_a_Nucleophilic_Aromatic_Substitution_Reaction/25015827