المؤلفون: Yang Yang, Xiangfei Geng, Zhiming Wu, Bin Ding, Weidong Liu, Qun Zhang, Baoshan Guan

مصطلحات موضوعية: Physiology, Biotechnology, Ecology, Inorganic Chemistry, Space Science, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, wettability alteration effect, unique interfacial properties, scanning electron microscopy, high cost limits, attracted considerable attention, 23 – 4, oil displacement agent, enhancing oil recovery, amphiphilic magnesium hydroxide, elastic film could, additional oil could, wet solid surface, low amh concentration, ultralow concentration, amphiphilic groups, emulsions could, thickness size, thermogravimetric analysis, surface modification, scale applications, plane size, mild conditions, heterogeneous core

العلاقة: https://figshare.com/articles/journal_contribution/Amphiphilic_Magnesium_Hydroxide_Nanosheets_for_Enhanced_Oil_Recovery/24539504Test

الإتاحة: https://doi.org/10.1021/acsanm.3c03982.s001Test
https://figshare.com/articles/journal_contribution/Amphiphilic_Magnesium_Hydroxide_Nanosheets_for_Enhanced_Oil_Recovery/24539504Test

المؤلفون: Jinwei Yuan, Lu Shen, Na Guo, Yanli Yin, Pengyuan Yang, Liangru Yang, Yongmei Xiao, Shouren Zhang

مصطلحات موضوعية: Biochemistry, Microbiology, Cell Biology, Genetics, Molecular Biology, Physiology, Biotechnology, Chemical Sciences not elsewhere classified, dmso – h, oac )< sub, induced cascade cyclization, 1 ‑ acryloyl, 2 , induced phi, cyclization reaction, room temperature, provide good, mild conditions, green medium, excellent yields, difluoroalkylated pyrrolo, >] indolediones, 2 ‑<, 2 -<

العلاقة: https://figshare.com/articles/journal_contribution/Visible-Light-Induced_Cascade_Cyclization_of_1_Acryloyl-2-cyanoindole_Access_of_Difluoroalkylated_Pyrrolo_1_2_i_a_i_indolediones/24545407Test

الإتاحة: https://doi.org/10.1021/acs.joc.3c02183.s001Test
https://figshare.com/articles/journal_contribution/Visible-Light-Induced_Cascade_Cyclization_of_1_Acryloyl-2-cyanoindole_Access_of_Difluoroalkylated_Pyrrolo_1_2_i_a_i_indolediones/24545407Test

المؤلفون: Prahallad Meher, Satya Prakash Panda, Sanat Kumar Mahapatra, Karan Ramdas Thombare, Lisa Roy, Sandip Murarka

مصطلحات موضوعية: Biochemistry, Cell Biology, Molecular Biology, Pharmacology, Biotechnology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, Information Systems not elsewhere classified, dairs enables arylation, triphenyl phosphine, reaction mechanism, practical mode, n <, mild conditions, excellent yields, diaryliodonium reagents, aryl assembly

العلاقة: https://figshare.com/articles/journal_contribution/A_General_Electron_Donor_Acceptor_Photoactivation_Platform_of_Diaryliodonium_Reagents_Arylation_of_Heterocycles/24559791Test

الإتاحة: https://doi.org/10.1021/acs.orglett.3c03365.s001Test
https://figshare.com/articles/journal_contribution/A_General_Electron_Donor_Acceptor_Photoactivation_Platform_of_Diaryliodonium_Reagents_Arylation_of_Heterocycles/24559791Test

المؤلفون: Mahesh S. Gadhave, Soumen Barik, Felix Wessels, Akkattu T. Biju

مصطلحات موضوعية: Biochemistry, Medicine, Molecular Biology, Neuroscience, Ecology, Marine Biology, Mental Health, Virology, Computational Biology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, mild conditions initiated, adventitious water present, carbenes underwent smooth, commercially available aldehydes, n , heterocyclic carbenes, practical route, functionalized isoindolin, excellent yields, annulation triggered

العلاقة: https://figshare.com/articles/journal_contribution/Nucleophilic_Acylation_Annulation_Cascade_of_2_Chlorobenzonitriles_Using_Aldehydes_Triggered_by_N_Heterocyclic_Carbenes/24559945Test

الإتاحة: https://doi.org/10.1021/acs.orglett.3c03376.s001Test
https://figshare.com/articles/journal_contribution/Nucleophilic_Acylation_Annulation_Cascade_of_2_Chlorobenzonitriles_Using_Aldehydes_Triggered_by_N_Heterocyclic_Carbenes/24559945Test

المؤلفون: Qi Lian, Jinke Chen, Kaipeng Huang, Keqiang Hou, Jiansong Fang, Wentao Wei, Jingwei Zhou

مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Ecology, Marine Biology, Space Science, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Physical Sciences not elsewhere classified, quantum mechanics computations, photoinduced oxidative n, photoinduced oxidative mechanism, mild conditions accompanied, aryl tertiary amines, alkaline environment based, alkaline environment, meticulous experiments

العلاقة: https://figshare.com/articles/journal_contribution/Alkali-Driven_Photoinduced_N_Dealkylation_of_Aryl_Tertiary_Amines_and_Amides/24565696Test

الإتاحة: https://doi.org/10.1021/acs.orglett.3c03519.s001Test
https://figshare.com/articles/journal_contribution/Alkali-Driven_Photoinduced_N_Dealkylation_of_Aryl_Tertiary_Amines_and_Amides/24565696Test

المؤلفون: Yiying Pang, Bowei Wang, Xiaoyi Gu, Huawei Shen, Xilong Yan, Yang Li, Ligong Chen

مصطلحات موضوعية: Biophysics, Biochemistry, Microbiology, Pharmacology, Biotechnology, Ecology, Developmental Biology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, via hydrogen bonding, also obviously enhance, efficient heterogeneous catalyst, abundant hydroxy groups, 2 , efficient catalysis, tailored cofs, pore channels, novel hydroxy, mild conditions, intramolecular five, green pathways, diverse substrates, desired products, cyclic carbonates

العلاقة: https://figshare.com/articles/journal_contribution/Hydroxy-Rich_Covalent_Organic_Framework_for_the_Efficient_Catalysis_of_the_Cycloaddition_of_CO_sub_2_sub_/24570155Test

الإتاحة: https://doi.org/10.1021/acs.langmuir.3c01719.s001Test
https://figshare.com/articles/journal_contribution/Hydroxy-Rich_Covalent_Organic_Framework_for_the_Efficient_Catalysis_of_the_Cycloaddition_of_CO_sub_2_sub_/24570155Test

المؤلفون: Yunfei Tian, Luping Zheng, Dongyu Guo, Yuyan Miao, Lijun Li, Weijun Fu, Zejiang Li

مصطلحات موضوعية: Biochemistry, Medicine, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, radical capture operations, good substrate scopes, could efficiently result, silanes photoinduced silylation, typical conditions, tolerated well, mild conditions, h <, gram level, diverse 3, bioactive molecule, >‑ indazoles, >- indazoles

العلاقة: https://figshare.com/articles/journal_contribution/Photopromoted_Free_Radical_Silylation_of_2_Aryl_2_i_H_i_indazoles_with_Silanes/24572788Test

الإتاحة: https://doi.org/10.1021/acs.joc.3c02232.s001Test
https://figshare.com/articles/journal_contribution/Photopromoted_Free_Radical_Silylation_of_2_Aryl_2_i_H_i_indazoles_with_Silanes/24572788Test

المؤلفون: Fang Xie, Jie Zhao, Deyue Ren, Jianming Xue, Jingyi Wang, Qin Zhao, Lu Liu, Xiaodan Liu

مصطلحات موضوعية: Biochemistry, Medicine, Molecular Biology, Neuroscience, Developmental Biology, Chemical Sciences not elsewhere classified, vicinal tetrasubstituted stereocenters, novel protocol features, existing reaction type, cyclic imino esters, broad substrate scope, rapid synthesis, mild conditions, high yields, h <, excellent levels, diastereoselective copper, chiral aziridines, catalyzed synthesis, catalyzed coupling, >- azirines

العلاقة: https://figshare.com/articles/journal_contribution/Enantio-_and_Diastereoselective_Copper-Catalyzed_Synthesis_of_Chiral_Aziridines_with_Vicinal_Tetrasubstituted_Stereocenters/24581933Test

الإتاحة: https://doi.org/10.1021/acs.orglett.3c03565.s001Test
https://figshare.com/articles/journal_contribution/Enantio-_and_Diastereoselective_Copper-Catalyzed_Synthesis_of_Chiral_Aziridines_with_Vicinal_Tetrasubstituted_Stereocenters/24581933Test

المؤلفون: Bingran Chen, Qinlin Chen, Yang Liu, Jinxiu Chen, Xi Zhou, Haifeng Wang, Qiongjiao Yan, Wei Wang, Zeyu Cai, Fen-Er Chen

مصطلحات موضوعية: Biochemistry, Medicine, Microbiology, Neuroscience, Physiology, Sociology, Developmental Biology, Mental Health, Space Science, Environmental Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, defluoroalkylation coupling reaction, >- trifluoroethyl hydroxylamine, >- difluoroallylated α, radical addition enabled, α , trifluoroethyl radical, radical addition, n <, gem <, trifluoromethyl alkenes, n -<, mild conditions, h shift, easy operation

العلاقة: https://figshare.com/articles/journal_contribution/Visible-Light-Induced_Defluorinative_C_sp_sup_3_sup_H_Alkylation_for_the_Synthesis_of_i_gem_i_-Difluoroallylated_Trifluoromethylamines/24584934Test

الإتاحة: https://doi.org/10.1021/acs.orglett.3c03523.s001Test
https://figshare.com/articles/journal_contribution/Visible-Light-Induced_Defluorinative_C_sp_sup_3_sup_H_Alkylation_for_the_Synthesis_of_i_gem_i_-Difluoroallylated_Trifluoromethylamines/24584934Test

المؤلفون: Viktor Eriksson, Leyla Beckerman, Erik Aerts, Markus Andersson Trojer, Lars Evenäs

مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Ecology, Inorganic Chemistry, Space Science, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, quartz crystal microbalance, diffusion coefficients fitted, responsive microcapsules pose, varying ph values, sharp ph transition, controlled triggered release, achieve controlled release, polyanhydride microcapsules exhibiting, microcapsules presented, polyanhydride poly, release measurements, spectrophotometric detection, physiological conditions, mild conditions, mass changes, external stimulus, dissipation monitoring, degradation products, degradation kinetics, correlate excellently, 9 allowed

العلاقة: https://figshare.com/articles/journal_contribution/Polyanhydride_Microcapsules_Exhibiting_a_Sharp_pH_Transition_at_Physiological_Conditions_for_Instantaneous_Triggered_Release/24584975Test

الإتاحة: https://doi.org/10.1021/acs.langmuir.3c02708.s001Test
https://figshare.com/articles/journal_contribution/Polyanhydride_Microcapsules_Exhibiting_a_Sharp_pH_Transition_at_Physiological_Conditions_for_Instantaneous_Triggered_Release/24584975Test