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Ultrahigh bandwidth spin noise spectroscopy: detection of large g-factor fluctuations in highly-n-doped GaAs.

Physical review letters

Berski F, Kuhn H, Lonnemann JG, Hübner J, Oestreich M.
PMID: 24237545
Phys Rev Lett. 2013 Nov 01;111(18):186602. doi: 10.1103/PhysRevLett.111.186602. Epub 2013 Oct 29.

We advance all optical spin noise spectroscopy (SNS) in semiconductors to detection bandwidths of several hundred gigahertz by employing a sophisticated scheme of pulse trains from ultrafast laser oscillators as an optical probe. The ultrafast SNS technique avoids the...

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Berski F, Kuhn H, Lonnemann JG, et al. Ultrahigh bandwidth spin noise spectroscopy: detection of large g-factor fluctuations in highly-n-doped GaAs. Phys Rev Lett. 2013;111(18):186602doi: 10.1103/PhysRevLett.111.186602.
Berski, F., Kuhn, H., Lonnemann, J. G., Hübner, J., & Oestreich, M. (2013). Ultrahigh bandwidth spin noise spectroscopy: detection of large g-factor fluctuations in highly-n-doped GaAs. Physical review letters, 111(18), 186602. https://doi.org/10.1103/PhysRevLett.111.186602
Berski, Fabian, et al. "Ultrahigh bandwidth spin noise spectroscopy: detection of large g-factor fluctuations in highly-n-doped GaAs." Physical review letters vol. 111,18 (2013): 186602. doi: https://doi.org/10.1103/PhysRevLett.111.186602
Berski F, Kuhn H, Lonnemann JG, Hübner J, Oestreich M. Ultrahigh bandwidth spin noise spectroscopy: detection of large g-factor fluctuations in highly-n-doped GaAs. Phys Rev Lett. 2013 Nov 01;111(18):186602. doi: 10.1103/PhysRevLett.111.186602. Epub 2013 Oct 29. PMID: 24237545.
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Bis(silylenyl)-substituted ferrocene-stabilized η.

Dalton transactions (Cambridge, England : 2003)

Luecke MP, Porwal D, Kostenko A, Zhou YP, Yao S, Keck M, Limberg C, Oestreich M, Driess M.
PMID: 28967014
Dalton Trans. 2017 Dec 21;46(47):16412-16418. doi: 10.1039/c7dt03301j. Epub 2017 Oct 02.

Reaction of FeX

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Luecke MP, Porwal D, Kostenko A, et al. Bis(silylenyl)-substituted ferrocene-stabilized η. Dalton Trans. 2017;46(47):16412-16418doi: 10.1039/c7dt03301j.
Luecke, M. P., Porwal, D., Kostenko, A., Zhou, Y. P., Yao, S., Keck, M., Limberg, C., Oestreich, M., & Driess, M. (2017). Bis(silylenyl)-substituted ferrocene-stabilized η. Dalton transactions (Cambridge, England : 2003), 46(47), 16412-16418. https://doi.org/10.1039/c7dt03301j
Luecke, Marcel-Philip, et al. "Bis(silylenyl)-substituted ferrocene-stabilized η." Dalton transactions (Cambridge, England : 2003) vol. 46,47 (2017): 16412-16418. doi: https://doi.org/10.1039/c7dt03301j
Luecke MP, Porwal D, Kostenko A, Zhou YP, Yao S, Keck M, Limberg C, Oestreich M, Driess M. Bis(silylenyl)-substituted ferrocene-stabilized η. Dalton Trans. 2017 Dec 21;46(47):16412-16418. doi: 10.1039/c7dt03301j. Epub 2017 Oct 02. PMID: 28967014.
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Phosphinic Amide as Directing Group Enabling Palladium(II)-Catalyzed ortho C-H Alkenylation of Anilines without and with Alkylation at the Nitrogen Atom.

Chemistry, an Asian journal

Jiao LY, Ferreira AV, Oestreich M.
PMID: 26370493
Chem Asian J. 2016 Feb 04;11(3):367-70. doi: 10.1002/asia.201500829. Epub 2015 Sep 24.

A phosphinic amide is introduced as a directing group for the ortho C-H alkenylation of anilines. The new donor group distinguishes itself from existing ones by assisting the C-H bond activation of anilides without (NH group) and with alkylation...

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Jiao LY, Ferreira AV, Oestreich M. Phosphinic Amide as Directing Group Enabling Palladium(II)-Catalyzed ortho C-H Alkenylation of Anilines without and with Alkylation at the Nitrogen Atom. Chem Asian J. 2015;11(3):367-70doi: 10.1002/asia.201500829.
Jiao, L. Y., Ferreira, A. V., & Oestreich, M. (2016). Phosphinic Amide as Directing Group Enabling Palladium(II)-Catalyzed ortho C-H Alkenylation of Anilines without and with Alkylation at the Nitrogen Atom. Chemistry, an Asian journal, 11(3), 367-70. https://doi.org/10.1002/asia.201500829
Jiao, Lin-Yu, et al. "Phosphinic Amide as Directing Group Enabling Palladium(II)-Catalyzed ortho C-H Alkenylation of Anilines without and with Alkylation at the Nitrogen Atom." Chemistry, an Asian journal vol. 11,3 (2016): 367-70. doi: https://doi.org/10.1002/asia.201500829
Jiao LY, Ferreira AV, Oestreich M. Phosphinic Amide as Directing Group Enabling Palladium(II)-Catalyzed ortho C-H Alkenylation of Anilines without and with Alkylation at the Nitrogen Atom. Chem Asian J. 2016 Feb 04;11(3):367-70. doi: 10.1002/asia.201500829. Epub 2015 Sep 24. PMID: 26370493.
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Asymmetric catalysis with silicon-based cuprates: enantio- and regioselective allylic substitution of linear precursors.

Chemistry (Weinheim an der Bergstrasse, Germany)

Hensel A, Oestreich M.
PMID: 25965581
Chemistry. 2015 Jun 15;21(25):9062-5. doi: 10.1002/chem.201501371. Epub 2015 May 12.

An enantio- and regioselective allylic silylation of linear allylic phosphates that makes use of catalytically generated cuprate-type silicon nucleophiles is reported. The method relies on soft bis(triorganosilyl) zincs as silicon pronucleophiles that are prepared in situ from the corresponding...

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Hensel A, Oestreich M. Asymmetric catalysis with silicon-based cuprates: enantio- and regioselective allylic substitution of linear precursors. Chemistry. 2015;21(25):9062-5doi: 10.1002/chem.201501371.
Hensel, A., & Oestreich, M. (2015). Asymmetric catalysis with silicon-based cuprates: enantio- and regioselective allylic substitution of linear precursors. Chemistry (Weinheim an der Bergstrasse, Germany), 21(25), 9062-5. https://doi.org/10.1002/chem.201501371
Hensel, Alexander, and Oestreich, Martin. "Asymmetric catalysis with silicon-based cuprates: enantio- and regioselective allylic substitution of linear precursors." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,25 (2015): 9062-5. doi: https://doi.org/10.1002/chem.201501371
Hensel A, Oestreich M. Asymmetric catalysis with silicon-based cuprates: enantio- and regioselective allylic substitution of linear precursors. Chemistry. 2015 Jun 15;21(25):9062-5. doi: 10.1002/chem.201501371. Epub 2015 May 12. PMID: 25965581.
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Erratum: Ultrahigh Bandwidth Spin Noise Spectroscopy: Detection of Large g-Factor Fluctuations in Highly-n-Doped GaAs [Phys. Rev. Lett. 111, 186602 (2013)].

Physical review letters

Berski F, Kuhn H, Lonnemann JG, Hübner J, Oestreich M.
PMID: 26991207
Phys Rev Lett. 2016 Mar 04;116(9):099901. doi: 10.1103/PhysRevLett.116.099901. Epub 2016 Mar 03.

This corrects the article DOI: 10.1103/PhysRevLett.111.186602.

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Berski F, Kuhn H, Lonnemann JG, et al. Erratum: Ultrahigh Bandwidth Spin Noise Spectroscopy: Detection of Large g-Factor Fluctuations in Highly-n-Doped GaAs [Phys. Rev. Lett. 111, 186602 (2013)]. Phys Rev Lett. 2016;116(9):099901doi: 10.1103/PhysRevLett.116.099901.
Berski, F., Kuhn, H., Lonnemann, J. G., Hübner, J., & Oestreich, M. (2016). Erratum: Ultrahigh Bandwidth Spin Noise Spectroscopy: Detection of Large g-Factor Fluctuations in Highly-n-Doped GaAs [Phys. Rev. Lett. 111, 186602 (2013)]. Physical review letters, 116(9), 099901. https://doi.org/10.1103/PhysRevLett.116.099901
Berski, Fabian, et al. "Erratum: Ultrahigh Bandwidth Spin Noise Spectroscopy: Detection of Large g-Factor Fluctuations in Highly-n-Doped GaAs [Phys. Rev. Lett. 111, 186602 (2013)]." Physical review letters vol. 116,9 (2016): 099901. doi: https://doi.org/10.1103/PhysRevLett.116.099901
Berski F, Kuhn H, Lonnemann JG, Hübner J, Oestreich M. Erratum: Ultrahigh Bandwidth Spin Noise Spectroscopy: Detection of Large g-Factor Fluctuations in Highly-n-Doped GaAs [Phys. Rev. Lett. 111, 186602 (2013)]. Phys Rev Lett. 2016 Mar 04;116(9):099901. doi: 10.1103/PhysRevLett.116.099901. Epub 2016 Mar 03. PMID: 26991207.
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Friedel-Crafts-Type Intermolecular C-H Silylation of Electron-Rich Arenes Initiated by Base-Metal Salts.

Angewandte Chemie (International ed. in English)

Yin Q, Klare HF, Oestreich M.
PMID: 26821860
Angew Chem Int Ed Engl. 2016 Feb 24;55(9):3204-7. doi: 10.1002/anie.201510469. Epub 2016 Jan 28.

An electrophilic aromatic substitution (SE Ar) with a catalytically generated silicon electrophile is reported. Essentially any commercially available base-metal salt acts as an initiator/catalyst when activated with NaBAr(F)4. The thus-generated Lewis acid then promotes the SE Ar of electron-rich...

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Yin Q, Klare HF, Oestreich M. Friedel-Crafts-Type Intermolecular C-H Silylation of Electron-Rich Arenes Initiated by Base-Metal Salts. Angew Chem Int Ed Engl. 2016;55(9):3204-7doi: 10.1002/anie.201510469.
Yin, Q., Klare, H. F., & Oestreich, M. (2016). Friedel-Crafts-Type Intermolecular C-H Silylation of Electron-Rich Arenes Initiated by Base-Metal Salts. Angewandte Chemie (International ed. in English), 55(9), 3204-7. https://doi.org/10.1002/anie.201510469
Yin, Qin, et al. "Friedel-Crafts-Type Intermolecular C-H Silylation of Electron-Rich Arenes Initiated by Base-Metal Salts." Angewandte Chemie (International ed. in English) vol. 55,9 (2016): 3204-7. doi: https://doi.org/10.1002/anie.201510469
Yin Q, Klare HF, Oestreich M. Friedel-Crafts-Type Intermolecular C-H Silylation of Electron-Rich Arenes Initiated by Base-Metal Salts. Angew Chem Int Ed Engl. 2016 Feb 24;55(9):3204-7. doi: 10.1002/anie.201510469. Epub 2016 Jan 28. PMID: 26821860.
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Catalytic Friedel-Crafts C-H Borylation of Electron-Rich Arenes: Dramatic Rate Acceleration by Added Alkenes.

Angewandte Chemie (International ed. in English)

Yin Q, Klare HF, Oestreich M.
PMID: 28244623
Angew Chem Int Ed Engl. 2017 Mar 20;56(13):3712-3717. doi: 10.1002/anie.201611536. Epub 2017 Feb 28.

In the electrophilic C-H borylation of electron-rich aromatic compounds with catecholborane, the catalytic generation of the boron electrophile is initiated by heterolysis of the B-H bond by various Lewis and Brønsted acids, with a boronium ion formed exclusively. After...

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Yin Q, Klare HF, Oestreich M. Catalytic Friedel-Crafts C-H Borylation of Electron-Rich Arenes: Dramatic Rate Acceleration by Added Alkenes. Angew Chem Int Ed Engl. 2017;56(13):3712-3717doi: 10.1002/anie.201611536.
Yin, Q., Klare, H. F., & Oestreich, M. (2017). Catalytic Friedel-Crafts C-H Borylation of Electron-Rich Arenes: Dramatic Rate Acceleration by Added Alkenes. Angewandte Chemie (International ed. in English), 56(13), 3712-3717. https://doi.org/10.1002/anie.201611536
Yin, Qin, et al. "Catalytic Friedel-Crafts C-H Borylation of Electron-Rich Arenes: Dramatic Rate Acceleration by Added Alkenes." Angewandte Chemie (International ed. in English) vol. 56,13 (2017): 3712-3717. doi: https://doi.org/10.1002/anie.201611536
Yin Q, Klare HF, Oestreich M. Catalytic Friedel-Crafts C-H Borylation of Electron-Rich Arenes: Dramatic Rate Acceleration by Added Alkenes. Angew Chem Int Ed Engl. 2017 Mar 20;56(13):3712-3717. doi: 10.1002/anie.201611536. Epub 2017 Feb 28. PMID: 28244623.
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Cooperative Catalysis at Metal-Sulfur Bonds.

Accounts of chemical research

Omann L, Königs CDF, Klare HFT, Oestreich M.
PMID: 28406290
Acc Chem Res. 2017 May 16;50(5):1258-1269. doi: 10.1021/acs.accounts.7b00089. Epub 2017 Apr 13.

Cooperative catalysis has attracted tremendous attention in recent years, emerging as a key strategy for the development of novel atom-economic and environmentally more benign catalytic processes. In particular, Noyori-type complexes with metal-nitrogen bonds have been extensively studied and evolved...

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Omann L, Königs CDF, Klare HFT, et al. Cooperative Catalysis at Metal-Sulfur Bonds. Acc Chem Res. 2017;50(5):1258-1269doi: 10.1021/acs.accounts.7b00089.
Omann, L., Königs, C. D. F., Klare, H. F. T., & Oestreich, M. (2017). Cooperative Catalysis at Metal-Sulfur Bonds. Accounts of chemical research, 50(5), 1258-1269. https://doi.org/10.1021/acs.accounts.7b00089
Omann, Lukas, et al. "Cooperative Catalysis at Metal-Sulfur Bonds." Accounts of chemical research vol. 50,5 (2017): 1258-1269. doi: https://doi.org/10.1021/acs.accounts.7b00089
Omann L, Königs CDF, Klare HFT, Oestreich M. Cooperative Catalysis at Metal-Sulfur Bonds. Acc Chem Res. 2017 May 16;50(5):1258-1269. doi: 10.1021/acs.accounts.7b00089. Epub 2017 Apr 13. PMID: 28406290.
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Hydrogenation and Transfer Hydrogenation Promoted by Tethered Ru-S Complexes: From Cooperative Dihydrogen Activation to Hydride Abstraction/Proton Release from Dihydrogen Surrogates.

Chemistry (Weinheim an der Bergstrasse, Germany)

Lefranc A, Qu ZW, Grimme S, Oestreich M.
PMID: 27311877
Chemistry. 2016 Jul 11;22(29):10009-16. doi: 10.1002/chem.201600386. Epub 2016 Jun 17.

Hydrogenation and transfer hydrogenation of imines with cyclohexa-1,4-dienes, as well as with a representative Hantzsch ester dihydrogen surrogate, are reported. Both processes are catalyzed by tethered Ru-S complexes but differ in the activation mode of the dihydrogen source: cooperative...

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Lefranc A, Qu ZW, Grimme S, et al. Hydrogenation and Transfer Hydrogenation Promoted by Tethered Ru-S Complexes: From Cooperative Dihydrogen Activation to Hydride Abstraction/Proton Release from Dihydrogen Surrogates. Chemistry. 2016;22(29):10009-16doi: 10.1002/chem.201600386.
Lefranc, A., Qu, Z. W., Grimme, S., & Oestreich, M. (2016). Hydrogenation and Transfer Hydrogenation Promoted by Tethered Ru-S Complexes: From Cooperative Dihydrogen Activation to Hydride Abstraction/Proton Release from Dihydrogen Surrogates. Chemistry (Weinheim an der Bergstrasse, Germany), 22(29), 10009-16. https://doi.org/10.1002/chem.201600386
Lefranc, Alice, et al. "Hydrogenation and Transfer Hydrogenation Promoted by Tethered Ru-S Complexes: From Cooperative Dihydrogen Activation to Hydride Abstraction/Proton Release from Dihydrogen Surrogates." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 22,29 (2016): 10009-16. doi: https://doi.org/10.1002/chem.201600386
Lefranc A, Qu ZW, Grimme S, Oestreich M. Hydrogenation and Transfer Hydrogenation Promoted by Tethered Ru-S Complexes: From Cooperative Dihydrogen Activation to Hydride Abstraction/Proton Release from Dihydrogen Surrogates. Chemistry. 2016 Jul 11;22(29):10009-16. doi: 10.1002/chem.201600386. Epub 2016 Jun 17. PMID: 27311877.
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Access to Fully Alkylated Germanes by B(C.

Organic letters

Keess S, Oestreich M.
PMID: 28358201
Org Lett. 2017 Apr 07;19(7):1898-1901. doi: 10.1021/acs.orglett.7b00672. Epub 2017 Mar 30.

Various cyclohexa-2,5-dien-1-yl-substituted germanes are shown to serve as easy-to-handle surrogates of hydrogermanes, including gaseous MeGeH

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Keess S, Oestreich M. Access to Fully Alkylated Germanes by B(C. Org Lett. 2017;19(7):1898-1901doi: 10.1021/acs.orglett.7b00672.
Keess, S., & Oestreich, M. (2017). Access to Fully Alkylated Germanes by B(C. Organic letters, 19(7), 1898-1901. https://doi.org/10.1021/acs.orglett.7b00672
Keess, Sebastian, and Oestreich, Martin. "Access to Fully Alkylated Germanes by B(C." Organic letters vol. 19,7 (2017): 1898-1901. doi: https://doi.org/10.1021/acs.orglett.7b00672
Keess S, Oestreich M. Access to Fully Alkylated Germanes by B(C. Org Lett. 2017 Apr 07;19(7):1898-1901. doi: 10.1021/acs.orglett.7b00672. Epub 2017 Mar 30. PMID: 28358201.
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[Late psychic-mental-social maturation of a 6-year-old girl].

Praxis der Kinderpsychologie und Kinderpsychiatrie

OESTREICH G.
PMID: 14481191
Prax Kinderpsychol Kinderpsychiatr. 1962 May-Jun;11:138-50.

No abstract available.

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OESTREICH G. [Late psychic-mental-social maturation of a 6-year-old girl]. Prax Kinderpsychol Kinderpsychiatr. 1962;11:138-50
OESTREICH, G. (1962). [Late psychic-mental-social maturation of a 6-year-old girl]. Praxis der Kinderpsychologie und Kinderpsychiatrie, 11138-50.
OESTREICH, G. "[Late psychic-mental-social maturation of a 6-year-old girl]." Praxis der Kinderpsychologie und Kinderpsychiatrie vol. 11 (1962): 138-50.
OESTREICH G. [Late psychic-mental-social maturation of a 6-year-old girl]. Prax Kinderpsychol Kinderpsychiatr. 1962 May-Jun;11:138-50. German. PMID: 14481191.
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"True" chirality transfer from silicon to carbon: asymmetric amplification in a reagent-controlled palladium-catalyzed hydrosilylation.

Angewandte Chemie (International ed. in English)

Oestreich M, Rendler S.
PMID: 15742322
Angew Chem Int Ed Engl. 2005 Mar 04;44(11):1661-4. doi: 10.1002/anie.200462355.

No abstract available.

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Oestreich M, Rendler S. "True" chirality transfer from silicon to carbon: asymmetric amplification in a reagent-controlled palladium-catalyzed hydrosilylation. Angew Chem Int Ed Engl. 2005;44(11):1661-4doi: 10.1002/anie.200462355.
Oestreich, M., & Rendler, S. (2005). "True" chirality transfer from silicon to carbon: asymmetric amplification in a reagent-controlled palladium-catalyzed hydrosilylation. Angewandte Chemie (International ed. in English), 44(11), 1661-4. https://doi.org/10.1002/anie.200462355
Oestreich, Martin, and Rendler, Sebastian. ""True" chirality transfer from silicon to carbon: asymmetric amplification in a reagent-controlled palladium-catalyzed hydrosilylation." Angewandte Chemie (International ed. in English) vol. 44,11 (2005): 1661-4. doi: https://doi.org/10.1002/anie.200462355
Oestreich M, Rendler S. "True" chirality transfer from silicon to carbon: asymmetric amplification in a reagent-controlled palladium-catalyzed hydrosilylation. Angew Chem Int Ed Engl. 2005 Mar 04;44(11):1661-4. doi: 10.1002/anie.200462355. PMID: 15742322.
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Showing 1 to 12 of 234 entries