المؤلفون: Lin-Lin Ma, You Zhou, Yong-Xing Tang, Ting Chen, Zheng-Hao Wang, Yan-Dong Wu, Jun-Gang Wang, An-Xin Wu

مصطلحات موضوعية: Biochemistry, Genetics, Molecular Biology, Physiology, Pharmacology, Biotechnology, Chemical Sciences not elsewhere classified, potentially enriching bioactive, efficient synthetic method, >] indazole skeletons, >] indazole derivatives, constructing related molecules, constructing 2, reaction conditions, new methodology, molecule libraries, disubstituted pyrimido, disubstituted pyrimidio, controlled regioselective, b <, 60 pyrimidio

Relation: https://figshare.com/articles/journal_contribution/I_sub_2_sub_DMSO-Mediated_Construction_of_2_3-_and_2_4-Disubstituted_Pyrimido_1_2_i_b_i_indazole_Skeletons/25315556

الاتاحة: https://doi.org/10.1021/acs.joc.3c02761.s001
https://figshare.com/articles/journal_contribution/I_sub_2_sub_DMSO-Mediated_Construction_of_2_3-_and_2_4-Disubstituted_Pyrimido_1_2_i_b_i_indazole_Skeletons/25315556

المؤلفون: Lin-Lin Ma, You Zhou, Yong-Xing Tang, Ting Chen, Zheng-Hao Wang, Yan-Dong Wu, Jun-Gang Wang, An-Xin Wu

مصطلحات موضوعية: Biochemistry, Genetics, Molecular Biology, Physiology, Pharmacology, Biotechnology, Chemical Sciences not elsewhere classified, potentially enriching bioactive, efficient synthetic method, >] indazole skeletons, >] indazole derivatives, constructing related molecules, constructing 2, reaction conditions, new methodology, molecule libraries, disubstituted pyrimido, disubstituted pyrimidio, controlled regioselective, b <, 60 pyrimidio

Relation: https://figshare.com/articles/journal_contribution/I_sub_2_sub_DMSO-Mediated_Construction_of_2_3-_and_2_4-Disubstituted_Pyrimido_1_2_i_b_i_indazole_Skeletons/25315556

الاتاحة: https://doi.org/10.1021/acs.joc.3c02761.s001

المؤلفون: María Álvarez (3951581), Francisco Molina (4028669), Pedro J. Pérez (1621264)

مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Genetics, Neuroscience, Biotechnology, Cancer, Mental Health, Physical Sciences not elsewhere classified, silver catalysis control, directing groups ), via carbene transfer, linear alkanes c, 2 , controlled regioselective functionalization, linear alkanes, controlled strategy, unprecedented level, secondary sites, mainly governed, large differences, electronic properties, diazo reagent, diazo compounds, alternative approach

Relation: https://figshare.com/articles/journal_contribution/Carbene-Controlled_Regioselective_Functionalization_of_Linear_Alkanes_under_Silver_Catalysis/21720173

الاتاحة: https://doi.org/10.1021/jacs.2c11707.s001

المؤلفون: Sibin Wang (4988636), Oleksii Zhelavskyi (11614803), Jeonghyo Lee (4988639), Alonso J. Argüelles (1438951), Yaroslav Ya. Khomutnyk (11614806), Enoch Mensah (11614809), Hao Guo (346528), Rami Hourani (2164174), Paul M. Zimmerman (1275564), Pavel Nagorny (1438945)

مصطلحات موضوعية: Biophysics, Biochemistry, Biotechnology, Immunology, Chemical Sciences not elsewhere classified, two reaction mechanisms, steric factors responsible, regiodivergent fashion depending, observed c2 selectivities, nondeuterated substrates revealed, differentially protected saccharides, anomeric phosphate intermediate, >- addition products, >- addition mechanism, 6 differentially protected, controlled regioselective acetalization, pot telescoped procedures, computational studies indicate, article describes studies, 1 mol %, controlled regioselective acetalizations, reused multiple times, immobilized polymeric variants, regioselective acetal protection, regioselective cpa, monomeric variants, catalyzed acetalizations, pot synthesis, derived 1, 1 rr

Relation: https://figshare.com/articles/journal_contribution/Studies_of_Catalyst-Controlled_Regioselective_Acetalization_and_Its_Application_to_Single-Pot_Synthesis_of_Differentially_Protected_Saccharides/16892190

الاتاحة: https://doi.org/10.1021/jacs.1c08448.s019

المؤلفون: Sibin Wang (4988636), Oleksii Zhelavskyi (11614803), Jeonghyo Lee (4988639), Alonso J. Argüelles (1438951), Yaroslav Ya. Khomutnyk (11614806), Enoch Mensah (11614809), Hao Guo (346528), Rami Hourani (2164174), Paul M. Zimmerman (1275564), Pavel Nagorny (1438945)

مصطلحات موضوعية: Biophysics, Biochemistry, Biotechnology, Immunology, Chemical Sciences not elsewhere classified, two reaction mechanisms, steric factors responsible, regiodivergent fashion depending, observed c2 selectivities, nondeuterated substrates revealed, differentially protected saccharides, anomeric phosphate intermediate, >- addition products, >- addition mechanism, 6 differentially protected, controlled regioselective acetalization, pot telescoped procedures, computational studies indicate, article describes studies, 1 mol %, controlled regioselective acetalizations, reused multiple times, immobilized polymeric variants, regioselective acetal protection, regioselective cpa, monomeric variants, catalyzed acetalizations, pot synthesis, derived 1, 1 rr

Relation: https://figshare.com/articles/journal_contribution/Studies_of_Catalyst-Controlled_Regioselective_Acetalization_and_Its_Application_to_Single-Pot_Synthesis_of_Differentially_Protected_Saccharides/16892187

الاتاحة: https://doi.org/10.1021/jacs.1c08448.s001

المؤلفون: Tereza Edlová (10526520), Hana Dvořáková (1677052), Václav Eigner (1590241), Tomáš Tobrman (1677046)

مصطلحات موضوعية: Biochemistry, Molecular Biology, Biotechnology, Computational Biology, Space Science, Chemical Sciences not elsewhere classified, disubstituted cyclobutenones, carbocation-stabilizing group, Substrate-Controlled Regioselective., Disubstituted, bromination reaction, disubstituted cyclobutenes, disubstituted 3- bromocyclobutenes, allylic position

Relation: https://figshare.com/articles/journal_contribution/Substrate-Controlled_Regioselective_Bromination_of_1_2-Disubstituted_Cyclobutenes_An_Application_in_the_Synthesis_of_2_3-Disubstituted_Cyclobutenones/14374098

الاتاحة: https://doi.org/10.1021/acs.joc.1c00261.s001

المؤلفون: Beibei Zhang (509356), Suyu Yang (8612379), Deqing Li (10276519), Mingtian Hao (10276522), Bo-Zhen Chen (2452408), Zengxi Li (1235676)

مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Biotechnology, Ecology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Ni 0 species, Ni center, ligand-controlled regioselective hy., DFT, CO 2 Controlled, C β ligating, CO 2, CO 2 insertion, C β atom, protonation

Relation: https://figshare.com/articles/journal_contribution/Insights_into_the_Regioselective_Hydrocarboxylation_of_Styrenes_with_CO_sub_2_sub_Controlled_by_the_Ligand_of_Nickel_Catalysts/14186653

الاتاحة: https://doi.org/10.1021/acssuschemeng.0c08845.s001

المؤلفون: Beibei Zhang (509356), Suyu Yang (8612379), Deqing Li (10276519), Mingtian Hao (10276522), Bo-Zhen Chen (2452408), Zengxi Li (1235676)

مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Biotechnology, Ecology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, Ni 0 species, Ni center, ligand-controlled regioselective hy., DFT, CO 2 Controlled, C β ligating, CO 2, CO 2 insertion, C β atom, protonation

Relation: https://figshare.com/articles/dataset/Insights_into_the_Regioselective_Hydrocarboxylation_of_Styrenes_with_CO_sub_2_sub_Controlled_by_the_Ligand_of_Nickel_Catalysts/14186656

الاتاحة: https://doi.org/10.1021/acssuschemeng.0c08845.s002

المؤلفون: Xian He, Xiang-Ai Yuan, Rui Tao, Xinru Zhang, Peng Liu, Siwei Bi

مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Molecular Biology, Biotechnology, Chemical Sciences not elsewhere classified, terminal alkynes provides, furnish valuable guidance, terminal alkynes catalyzed, interaction analyses show, l2 , l1 , controlled regioselective hydroacylation, catalyzed hydroacylation, repulsive interaction, controlled regioselectivity, unsaturated ketones, type mechanism, theoretical studies, steric effects, results demonstrate, refining reactions, reaction follows, linear selectivity, efficient strategy, branched selectivity

Relation: https://figshare.com/articles/journal_contribution/Theoretical_Studies_on_the_Mechanisms_and_Origins_of_Ligand-Controlled_Regioselective_Hydroacylation_of_Terminal_Alkynes_Catalyzed_by_the_Rhodium_I_Complex/24971819

الاتاحة: https://doi.org/10.1021/acs.organomet.3c00454.s001
https://figshare.com/articles/journal_contribution/Theoretical_Studies_on_the_Mechanisms_and_Origins_of_Ligand-Controlled_Regioselective_Hydroacylation_of_Terminal_Alkynes_Catalyzed_by_the_Rhodium_I_Complex/24971819

المؤلفون: Xian He, Xiang-Ai Yuan, Rui Tao, Xinru Zhang, Peng Liu, Siwei Bi

مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Molecular Biology, Biotechnology, Chemical Sciences not elsewhere classified, terminal alkynes provides, furnish valuable guidance, terminal alkynes catalyzed, interaction analyses show, l2 , l1 , controlled regioselective hydroacylation, catalyzed hydroacylation, repulsive interaction, controlled regioselectivity, unsaturated ketones, type mechanism, theoretical studies, steric effects, results demonstrate, refining reactions, reaction follows, linear selectivity, efficient strategy, branched selectivity

Relation: https://figshare.com/articles/dataset/Theoretical_Studies_on_the_Mechanisms_and_Origins_of_Ligand-Controlled_Regioselective_Hydroacylation_of_Terminal_Alkynes_Catalyzed_by_the_Rhodium_I_Complex/24971822

الاتاحة: https://doi.org/10.1021/acs.organomet.3c00454.s002
https://figshare.com/articles/dataset/Theoretical_Studies_on_the_Mechanisms_and_Origins_of_Ligand-Controlled_Regioselective_Hydroacylation_of_Terminal_Alkynes_Catalyzed_by_the_Rhodium_I_Complex/24971822