المؤلفون: Stammers, Ellie

المساهمون: Lennox, Alastair, Clayden, Jonathan

مصطلحات موضوعية: Biaryls, Reduction, Electrochemistry, Ureas

URL الوصول: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.876282

المؤلفون: Jie Zhang, Kun Wang, Can Zhu

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Genetics, Molecular Biology, Biotechnology, Evolutionary Biology, Cancer, Space Science, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, versatile chiral catalysts, racemizing biaryl skeletons, probably proceeds via, found crucial applications, enantioselectively formed together, cocrystal complex would, chiral ammonium salt, bulky alkyl substitution, bidentate diamine ligand, atropisomeric biaryls enabled, allows axial rotation, access chiral biaryls, ensure efficient racemization, efficient crystallization, transition metals, significantly accelerated, nicely recoverable, indispensable element, easily scalable

Relation: https://figshare.com/articles/journal_contribution/Deracemization_of_Atropisomeric_Biaryls_Enabled_by_Copper_Catalysis/25016664

الاتاحة: https://doi.org/10.1021/jacsau.3c00623.s001
https://figshare.com/articles/journal_contribution/Deracemization_of_Atropisomeric_Biaryls_Enabled_by_Copper_Catalysis/25016664

المؤلفون: Ye, Chen‐Xi, Chen, Shuming, Han, Feng, Xie, Xiulan, Ivlev, Sergei, Houk, KN, Meggers, Eric

المصدر: Angewandte Chemie International Edition. 59(32)

مصطلحات موضوعية: Inorganic Chemistry, Organic Chemistry, Chemical Sciences, atroposelective reactions, chiral biaryls, chiral-at-metal complexes, homogeneous catalysis, N-arylpyrroles, Chemical sciences

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/3mj108gs
https://escholarship.org/content/qt3mj108gs/qt3mj108gs.pdf

المؤلفون: Ye, Chen-Xi, Chen, Shuming, Han, Feng, Xie, Xiulan, Ivlev, Sergei, Houk, KN, Meggers, Eric

المصدر: Angewandte Chemie (International ed. in English). 59(32)

مصطلحات موضوعية: N-arylpyrroles, atroposelective reactions, chiral biaryls, chiral-at-metal complexes, homogeneous catalysis, Chemical Sciences, Organic Chemistry

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/3mj108gs

المؤلفون: Kyle G. Pearce, Chiara Dinoi, Ryan J. Schwamm, Laurent Maron, Mary F. Mahon, Michael S. Hill

المصدر: Advanced Science, Vol 10, Iss 31, Pp n/a-n/a (2023)

مصطلحات موضوعية: biaryls, calcium, density functional theory, main group chemistry, Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2198-3844

URL الوصول: https://doaj.org/article/b02a811e760b4b2e92d1a1bd02303a84

المؤلفون: Abdollahi-Alibeik Mohammad, Ramazani Zahra

المصدر: Main Group Metal Chemistry, Vol 45, Iss 1, Pp 190-201 (2022)

مصطلحات موضوعية: mcm-41, fe3o4, mesoporous silica, nanocatalyst, ullmann homocoupling, biaryls, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2191-0219

URL الوصول: https://doaj.org/article/30e41656a102458ba979c713758d9cfb

المؤلفون: Jangam Lakshmidevi, Bandameeda Ramesh Naidu, Katta Venkateswarlu, Marlia M. Hanafiah, Sivarama Krishna Lakkaboyana

المصدر: Green Chemistry Letters and Reviews, Vol 15, Iss 3, Pp 529-536 (2022)

مصطلحات موضوعية: CuCl-WEPA, waste volarization, (hetero)arylboronic acids, oxidative self-coupling, symmetrical biaryls, low E-factor, Science, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1751-8253; https://doaj.org/toc/1751-7192

URL الوصول: https://doaj.org/article/69a79b9c83a141138ddc411d46e2feac

المؤلفون: Shiguang Pan, Cong Gao, Jiatong Gui, Beibei Hu, Lifeng Gai, Changsheng Qiao, Chengwei Liu

المصدر: Arabian Journal of Chemistry, Vol 16, Iss 1, Pp 104410- (2023)

مصطلحات موضوعية: Palladium, Titanium Dioxide, Biaryls, Suzuki-Miyaura Reaction, Heterogeneous Catalysis, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S1878535222007262; https://doaj.org/toc/1878-5352

URL الوصول: https://doaj.org/article/624d536fc21f431da760b2623a768dbc

المؤلفون: Sanil, Gana, Krzeszewski, Maciej, Chaładaj, Wojciech, Danikiewicz, Witold, Knysh, Iryna, Dobrzycki, Łukasz, Staszewska‐krajewska, Olga, Cyrański, Michał, K, Jacquemin, Denis, D, Gryko, Daniel, T

المساهمون: Institute of Physics, Polish Academy of Sciences, Warsaw, Chimie Et Interdisciplinarité : Synthèse, Analyse, Modélisation (CEISAM), Institut de Chimie - CNRS Chimie (INC-CNRS)-Centre National de la Recherche Scientifique (CNRS)-Nantes université - UFR des Sciences et des Techniques (Nantes univ - UFR ST), Nantes Université - pôle Sciences et technologie, Nantes Université (Nantes Univ)-Nantes Université (Nantes Univ)-Nantes Université - pôle Sciences et technologie, Nantes Université (Nantes Univ)-Nantes Université (Nantes Univ), Institut universitaire de France (IUF), Ministère de l'Education nationale, de l’Enseignement supérieur et de la Recherche (M.E.N.E.S.R.), Institute of Organic Chemistry (IOC), Polska Akademia Nauk = Polish Academy of Sciences = Académie polonaise des sciences (PAN), ANR-20-CE29-0005,BSE-forces,Géométries dans l'état excité dans le formalisme de Bethe-Salpeter(2020)

المصدر: ISSN: 1433-7851.

مصطلحات موضوعية: Alkynes, Biaryls, Dyes/Pigments, Fluorescence, Heterocycles, [CHIM]Chemical Sciences

الاتاحة: https://hal.science/hal-04845253
https://hal.science/hal-04845253v1/document
https://hal.science/hal-04845253v1/file/Angew%20Chem%20Int%20Ed%20-%202023%20-%20Sanil%20-%20Gold%E2%80%90Catalyzed%201%202%E2%80%90Aryl%20Shift%20and%20Double%20Alkyne%20Benzannulation.pdf
https://doi.org/10.1002/anie.202311123

المؤلفون: Kasandra J. Brick, Meilin Q. Lim, Eric C. Keske

مصطلحات موضوعية: Biophysics, Biochemistry, Genetics, Developmental Biology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, ome )< sub, f nmr spectroscopy, 3 , 19 , situ analysis, simes ), reacts nonproductively, poor substrates, poor activity, phenyl trimethoxysilanes, outlined based, mechanistic proposal, high yields, heterocyclic carbene, biaryls products, believe explains, aryl trimethoxysilanes, aryl chlorides

Relation: https://figshare.com/articles/journal_contribution/_NHC_Pd_allyl_Cl_Precatalysts_in_The_Hiyama_Reaction_of_Aryl_Chlorides_with_Aryl_Trimethoxysilanes_A_Study_in_Side_Reactions/24539378

الاتاحة: https://doi.org/10.1021/acs.organomet.3c00312.s001
https://figshare.com/articles/journal_contribution/_NHC_Pd_allyl_Cl_Precatalysts_in_The_Hiyama_Reaction_of_Aryl_Chlorides_with_Aryl_Trimethoxysilanes_A_Study_in_Side_Reactions/24539378

المؤلفون: Qian-Hui Liu, Meng-Tong Zhang, Yi-Yao Han, Mo Zhang, Zhan-Hui Zhang

مصطلحات موضوعية: Biochemistry, Physiology, Pharmacology, Biotechnology, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, various symmetrical biaryls, scanning electron microscopy, mild reaction conditions, 2 , solvothermal method, room temperature, ray techniques, ray diffraction, photocatalytic homocoupling, excellent yields, driven homocoupling, catalytic process, catalytic efficiency, arenediazonium tetrafluoroborates

Relation: https://figshare.com/articles/journal_contribution/Recyclable_Copper_Indium_Sulfide_Quantum_Dots_for_Photocatalytic_Homocoupling_of_Arenediazonium_Tetrafluoroborates/24714645

الاتاحة: https://doi.org/10.1021/acssuschemeng.3c05163.s001
https://figshare.com/articles/journal_contribution/Recyclable_Copper_Indium_Sulfide_Quantum_Dots_for_Photocatalytic_Homocoupling_of_Arenediazonium_Tetrafluoroborates/24714645

المؤلفون: Jiali Wang, Yangbo Cui, Siqi Xie, Jun-Qi Zhang, Dandan Hu, Shihao Shuai, Chun Zhang, Hongjun Ren

مصطلحات موضوعية: Biophysics, Biochemistry, Pharmacology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, excellent functional tolerance, catalyzed decarboxylative cross, broad substrate scope, biologically active molecules, producing zinc reagents, straightforward late, stage modification, protocol exhibits, potential significance, polyfluorinated biaryls, efficient pathway, drug discovery, aryl bromides

Relation: https://figshare.com/articles/journal_contribution/Mild_Pd-Catalyzed_Decarboxylative_Cross-Coupling_of_Zinc_II_Polyfluorobenzoates_with_Aryl_Bromides_and_Nonaflates_Access_to_Polyfluorinated_Biaryls/24887025

الاتاحة: https://doi.org/10.1021/acs.orglett.3c03730.s001
https://figshare.com/articles/journal_contribution/Mild_Pd-Catalyzed_Decarboxylative_Cross-Coupling_of_Zinc_II_Polyfluorobenzoates_with_Aryl_Bromides_and_Nonaflates_Access_to_Polyfluorinated_Biaryls/24887025

المؤلفون: Marco Kruppa, Thomas J. J. Müller

المصدر: Catalysts; Volume 13; Issue 2; Pages: 350

مصطلحات موضوعية: sequential palladium catalysis, one-pot reactions, Masuda borylation, Suzuki coupling, (hetero)aryl halides, (hetero)biaryls, multicomponent reactions

وصف الملف: application/pdf

Relation: Catalysis in Organic and Polymer Chemistry; https://dx.doi.org/10.3390/catal13020350

الاتاحة: https://doi.org/10.3390/catal13020350

المؤلفون: Norrehed, Sara, 1982, Karlsson, Christoffer, 1986, Light, Mark E., Thapper, Anders, Huang, Ping, Gogoll, A, 1957

المصدر: Monatshefte fuer Chemie. 150(1):77-84

مصطلحات موضوعية: Biaryls, Crystal structure, Heterocycles, Oxidative coupling, biradicals, Chemistry with specialization in Organic Chemistry, Kemi med inriktning mot organisk kemi

وصف الملف: print

URL الوصول: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-364531
https://doi.org/10.1007/s00706-018-2298-4

المؤلفون: Asja A. Kroeger (7301300), Amir Karton (807944)

مصطلحات موضوعية: Biophysics, Biochemistry, Cancer, Infectious Diseases, Computational Biology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, versatile reagent 1, transition structure stabilization, perylene bisimide cyclophanes, less complementary reactants, heterobiaryl ligand quinap, dynamic kinetic resolutions, dependent chirality transfer, complementary transition structures, 8 – 73, high enantiomerization barriers, calculated enantiomerization barriers, 1 ′- binaphthyl, different biaryls decrease, axially chiral biaryls, many biaryl compounds, cyclophane may form, 2 ′- diol, enantiomerization pathways, binaphthyl scaffolds, upon complexation, systematic enantiomer, synthetic relevance

Relation: https://figshare.com/articles/journal_contribution/Perylene_Bisimide_Cyclophanes_as_Biaryl_Enantiomerization_Catalysts_Explorations_into_Catalysis_and_Host_Guest_Chirality_Transfer/18858585

الاتاحة: https://doi.org/10.1021/acs.joc.1c02719.s001

المؤلفون: Lucas Warmuth, Aaron Weiß, Marco Reinhardt, Anna Meschkov, Ute Schepers, Joachim Podlech

المصدر: Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 224-228 (2021)

مصطلحات موضوعية: biaryls, boronates, mycotoxins, polyketides, suzuki coupling, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

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

URL الوصول: https://doaj.org/article/f662e86fc1de42b7b8fc892163fabbfa

المؤلفون: Joanna Wencel-Delord, Françoise Colobert

المصدر: SynOpen, Vol 04, Iss 04, Pp 107-115 (2020)

مصطلحات موضوعية: atropisomeric axis, atropisomeric biaryls, c–h arylation, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2509-9396

URL الوصول: https://doaj.org/article/0940f77df3aa454d94daf45481786bd1

المؤلفون: Xixi Song, Yueteng Zhang, Peng Ji, Fanxun Zeng, Fangchao Bi, Wei Wang

المصدر: Green Synthesis and Catalysis, Vol 1, Iss 1, Pp 66-69 (2020)

مصطلحات موضوعية: Aminocatalysis, Biaryls, Cascade reactions, Diels-Alder reaction, Organocatalysis, Ynals, Chemical technology, TP1-1185, Biochemistry, QD415-436

وصف الملف: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S2666554920300016; https://doaj.org/toc/2666-5549

URL الوصول: https://doaj.org/article/b3cca40277884f839461698ef50819ba

المؤلفون: Yongsu Li, Bendu Pan, Xuefeng He, Wang Xia, Yaqi Zhang, Hao Liang, Chitreddy V. Subba Reddy, Rihui Cao, Liqin Qiu

المصدر: Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 966-973 (2020)

مصطلحات موضوعية: asymmetric catalysis, biaryls, monophosphine ligand, palladium catalyst, suzuki–miyaura couplings, Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

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

URL الوصول: https://doaj.org/article/f924bbce98a74a578cb4d01ef0bee783

المؤلفون: Dr. S.K. Mishra

المصدر: International Journal of Innovative Research in Engineering & Multidisciplinary Physical Sciences, 10(4), (2022-07-20)

مصطلحات موضوعية: asymmetric catalysis, axial chirality, biaryls, rhodium, [2+2+2] cycloaddition

Relation: https://doi.org/10.5281/zenodo.8240775; https://doi.org/10.5281/zenodo.8240776; oai:zenodo.org:8240776

الاتاحة: https://doi.org/10.5281/zenodo.8240776