المؤلفون: Weichao Xue, Martin Oestreich

المصدر: ACS Central Science, Vol 6, Iss 7, Pp 1070-1081 (2020)

مصطلحات موضوعية: Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2374-7951

URL الوصول: https://doaj.org/article/41c7fefa8f654335996fb44b5118057e

المؤلفون: Xichang Dong, Andreas Weickgenannt, Martin Oestreich

المصدر: Nature Communications, Vol 8, Iss 1, Pp 1-7 (2017)

مصطلحات موضوعية: Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2041-1723

URL الوصول: https://doaj.org/article/e506d0b7d1b545dcbd08d7a705017f56

المؤلفون: Francis Forster, Martin Oestreich

المصدر: CHIMIA, Vol 72, Iss 9 (2018)

مصطلحات موضوعية: C–h functionalization, Cooperative catalysis, Dehydrogenative couplings, Main-group electrophiles, Chemistry, QD1-999

وصف الملف: electronic resource

Relation: https://www.chimia.ch/chimia/article/view/1480; https://doaj.org/toc/0009-4293; https://doaj.org/toc/2673-2424

URL الوصول: https://doaj.org/article/dcb47ba2ff234ed78862a05f3d023075

المؤلفون: Sebastian Rendler, Martin Oestreich

المصدر: Beilstein Journal of Organic Chemistry, Vol 3, Iss 1, p 9 (2007)

مصطلحات موضوعية: Science, Organic chemistry, QD241-441

وصف الملف: electronic resource

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

URL الوصول: https://doaj.org/article/9680834f2207489dbb874d3a6192f935

المؤلفون: Daniel Brösamlen, Martin Oestreich

مصطلحات موضوعية: Biophysics, Biochemistry, Cell Biology, Molecular Biology, Biotechnology, Inorganic Chemistry, Infectious Diseases, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, mild protocols allow, directing group attached, group tolerance, selective synthesis, regiodivergent hydroalkylation, radical mechanism, nickel catalyst, method features, linear alkylsilanes, high functional, either branched, catalyzed hydroalkylation, broad scope, also reported

Relation: https://figshare.com/articles/journal_contribution/Ligand-Controlled_On_Off_Switch_of_a_Silicon-Tethered_Directing_Group_Enabling_the_Regiodivergent_Hydroalkylation_of_Vinylsilanes_under_Ni_H_Catalysis/24746783

الاتاحة: https://doi.org/10.1021/acs.orglett.3c03799.s001
https://figshare.com/articles/journal_contribution/Ligand-Controlled_On_Off_Switch_of_a_Silicon-Tethered_Directing_Group_Enabling_the_Regiodivergent_Hydroalkylation_of_Vinylsilanes_under_Ni_H_Catalysis/24746783

المؤلفون: Zhi-Yuan Zhao, Ming Cui, Anne A. Poletti, Elisabeth Irran, Martin Oestreich

مصطلحات موضوعية: Biochemistry, Pharmacology, Cancer, Computational Biology, Environmental Sciences not elsewhere classified, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, unsaturated acceptor allows, two contiguous stereocenters, selectively afford either, quaternary carbon atom, different chiral ligands, bearing carbon atom, highly congested environment, catalyzed conjugate monoborylation, highly enantio, thereby leading, syn <, subsequent 1, selective reaction, second borylation, remaining α, neopentylic position, formed boron, diborylated product, diastereoselective copper, cyclohexadienones containing, conjugate addition, boron nucleophiles, boron nucleophile

Relation: https://figshare.com/articles/journal_contribution/Desymmetrization_of_Cyclohexadienones_Containing_a_Quaternary_Carbon_Atom_by_Conjugate_Addition_of_Boron_Nucleophiles/24795025

الاتاحة: https://doi.org/10.1021/acscatal.3c04725.s001
https://figshare.com/articles/journal_contribution/Desymmetrization_of_Cyclohexadienones_Containing_a_Quaternary_Carbon_Atom_by_Conjugate_Addition_of_Boron_Nucleophiles/24795025

المؤلفون: Hua-Jie Jiang, Honghua Zuo, Min Zhu, Illia Sharanov, Elisabeth Irran, Hendrik F. T. Klare, Sofja Tshepelevitsh, Märt Lõkov, Ivo Leito, Martin Oestreich

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Microbiology, Molecular Biology, Pharmacology, Biotechnology, Plant Biology, Chemical Sciences not elsewhere classified, Information Systems not elsewhere classified, anionic units connected, >- carborates decorated, different chiral binol, chiral catalysts, sodium salt, polymeric structure, phosphonate ’, oxygen atom, moderately successful, k <, derived phosphonates, conjugate acids, combining experiments, closo <, brønsted acids, based phosphonates, >< sub,

Relation: https://figshare.com/articles/journal_contribution/Chiral_Carborane_Acids_Decorated_with_Binol-Based_Phosphonates_Synthesis_Characterization_and_Application/24852126

الاتاحة: https://doi.org/10.1021/acs.joc.3c02162.s001
https://figshare.com/articles/journal_contribution/Chiral_Carborane_Acids_Decorated_with_Binol-Based_Phosphonates_Synthesis_Characterization_and_Application/24852126

المؤلفون: Supriya Rej (3547988), Hendrik F. T. Klare (7870064), Martin Oestreich (1353330)

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Cell Biology, Immunology, Infectious Diseases, Virology, Computational Biology, Chemical Sciences not elsewhere classified, electrocyclic ring closure, cationic intermediate emerging, cascade eventually leads, ion regeneration followed, allenyl group contain, silylalkyl group, thereby initiating, silylium ion, octane skeleton, nazarov cyclizations, nazarov cyclization, excess hydrosilane, endo <, containing bicyclo, conjugated polyenes

Relation: https://figshare.com/articles/journal_contribution/The_3_Dendralene_Motif_as_an_Entry_into_Nazarov_Cyclizations_by_Silylium-Ion_Initiation/21824724

الاتاحة: https://doi.org/10.1021/acs.orglett.2c04166.s001

المؤلفون: Hua-Jie Jiang (5310239), Hendrik D. A. Simon (14305474), Elisabeth Irran (1606072), Hendrik F. T. Klare (7870064), Martin Oestreich (1353330)

مصطلحات موضوعية: Biophysics, Biochemistry, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, without deoxygenation prevails, stereochemical probe revealed, stereochemical analysis employing, refined mechanistic picture, new experimental data, free silylcarboxonium ions, experiments also contributed, experimental mechanistic analysis, acetonitrile suppresses overreduction, oxo complex based, carbonyl hydrosilylation catalyzed, oxo complex introduced, carbonyl hydrosilylation, hydrosilanes catalyzed, acetonitrile ligand, stereogenic hydrosilane, key intermediates, catalytic cycle

Relation: https://figshare.com/articles/journal_contribution/Experimental_Mechanistic_Analysis_of_Carbonyl_Hydrosilylation_Catalyzed_by_Abu-Omar_s_Rhenium_V_Oxo_Complex/21785332

الاتاحة: https://doi.org/10.1021/acs.organomet.2c00500.s001

المؤلفون: Supriya Rej (3547988), Hendrik F. T. Klare (7870064), Martin Oestreich (1353330)

مصطلحات موضوعية: Biochemistry, Microbiology, Cell Biology, Genetics, Biotechnology, Evolutionary Biology, Ecology, Developmental Biology, Marine Biology, Cancer, Infectious Diseases, Plant Biology, Computational Biology, Chemical Sciences not elsewhere classified, substituted allenes, silylated indane, selective formation, nazarov electrocyclization, initiator ratio, endo <, cyclized product, conventional 1

Relation: https://figshare.com/articles/journal_contribution/Silylium-Ion-Promoted_Hydrosilylation_of_Aryl-Substituted_Allenes_Interception_by_Cyclization_of_the_Allyl-Cation_Intermediate/19116217

الاتاحة: https://doi.org/10.1021/acs.orglett.2c00011.s001

المؤلفون: Daniel Brösamlen, Martin Oestreich

المصدر: Organic Letters. 25:1901-1906

مصطلحات موضوعية: Organic Chemistry, Physical and Theoretical Chemistry, Biochemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::09e0bebe2e48c092c8942e9e6b85cc45
https://doi.org/10.1021/acs.orglett.3c00410

المؤلفون: Hendrik Klare, Martin Oestreich, Honghua Zuo

المصدر: The Journal of Organic Chemistry. 88:4024-4027

مصطلحات موضوعية: Organic Chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::6beea35a64de5c1d9060e3d6e8d61984
https://doi.org/10.1021/acs.joc.3c00261

المؤلفون: Muliang Zhang, Jinghui Zhang, Martin Oestreich

المصدر: Nature Synthesis. 2:439-447

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0e2dc7a5ebb304950e3226c64fc0a54c
https://doi.org/10.1038/s44160-023-00256-z

المؤلفون: Tao He (23919), Hendrik F. T. Klare (7870064), Martin Oestreich (1353330)

مصطلحات موضوعية: Biophysics, Biochemistry, Cancer, Mental Health, Infectious Diseases, Virology, Computational Biology, Biological Sciences not elsewhere classified, Chemical Sciences not elsewhere classified, alkylated arenes results, productive “ proton, higher proton affinity, fast proton transfer, reactive benzyl bromides, primary alkyl bromides, stabilized silylium ion, benzyl bromides, proton scavenger, ion regeneration, wheland intermediate, substituted tetraorganosilane, stoichiometric amounts, simple phenyl, silylated compared, ipso <, improved protocol, halogenated derivatives, also found

Relation: https://figshare.com/articles/journal_contribution/Silylium-Ion_Regeneration_by_Protodesilylation_Enables_Friedel_Crafts_Alkylation_with_Less_Isomerization_and_No_Defunctionalization/16632311

الاتاحة: https://doi.org/10.1021/acscatal.1c03602.s001

المؤلفون: Zaneta Papadopulu (9917312), Novid Kazeroonian (11819717), Elisabeth Irran (1606072), Martin Oestreich (1353330)

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Biotechnology, Immunology, Infectious Diseases, Computational Biology, Chemical Sciences not elsewhere classified, vicinal quaternary stereocenter, quaternary carbon atom, diastereomerically enriched form, cu – h, catalyzed enantioselective silylation, acyclic secondary alcohols, β ‑ position, secondary alcohols, catalyzed silylation, stereoisomeric mixtures, silyl ether, reacting stereoisomer, obtained motif, kinetic resolution, hydroxy group

Relation: https://figshare.com/articles/journal_contribution/One_out_of_Four_Kinetic_Resolution_of_Stereoisomeric_Mixtures_of_Secondary_Alcohols_with_a_Quaternary_Carbon_Atom_in_the_Position_by_Cu_H-Catalyzed_Enantioselective_Silylation/17153510

الاتاحة: https://doi.org/10.1021/acsorginorgau.1c00050.s001

المؤلفون: Yan Xu (14594), Hong Yi (172291), Martin Oestreich (1353330)

مصطلحات موضوعية: Biophysics, Biochemistry, Medicine, Cell Biology, Molecular Biology, Biotechnology, Immunology, Chemical Sciences not elsewhere classified, Allenylsilane, silyl group, bond formation, Bromide, Racemic, regioselectivity, Regioselective Synthesis, Silylated, enantioconvergent nickel-catalyzed ., enantioselection, Propargylic, chiral Pybox ligand, synthesis, racemic α- silylated propargylic br., Nickel-Catalyzed, Cross-Coupling, enantioenriched allenylsilanes, γ- position, propargyl electrophile, Enantioconvergent

Relation: https://figshare.com/articles/journal_contribution/Enantioconvergent_and_Regioselective_Synthesis_of_Allenylsilanes_by_Nickel-Catalyzed_C_sp_sup_2_sup_C_sp_sup_3_sup_Cross-Coupling_Starting_from_Racemic_Silylated_Propargylic_Bromides/14378507

الاتاحة: https://doi.org/10.1021/acs.organomet.1c00112.s001

المؤلفون: Tao He, Hendrik F. T. Klare, Martin Oestreich

المصدر: Journal of the American Chemical Society. 145:3795-3801

مصطلحات موضوعية: Colloid and Surface Chemistry, General Chemistry, Biochemistry, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::64a13dcf6daf451bdeb80beda223b134
https://doi.org/10.1021/jacs.2c13341

المؤلفون: Hendrik Klare, Haopeng Gao, Martin Oestreich, Avijit Roy

المصدر: Synthesis. 55:1602-1612

مصطلحات موضوعية: Organic Chemistry, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::26289399537a635cf305fe3ef91bffd7
https://doi.org/10.1055/a-2009-8114

المؤلفون: Martin Oestreich, Nektarios Kranidiotis-Hisatomi

المصدر: Synthesis. 55:1497-1506

مصطلحات موضوعية: Organic Chemistry, Catalysis

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::69e904631771140ca17a6ec609596a1c
https://doi.org/10.1055/a-2006-9754

المؤلفون: Yuanjiu Xiao, Lei Tang, Tong-Tong Xu, Jiang-Yi-Hui Sheng, Zhongyan Zhou, Lei Yue, Guoqiang Wang, Martin Oestreich, Jian-Jun Feng

المصدر: Chemical Science. 14:5608-5618

مصطلحات موضوعية: General Chemistry

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::a9203f648d99a1f6f850af682cf1f39b
https://doi.org/10.1039/d3sc01394d