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Reactivity of NHC Alane Adducts towards N-Heterocyclic Carbenes and Cyclic (Alkyl)(amino)carbenes: Ring Expansion, Ring Opening, and Al-H Bond Activation.

Chemistry (Weinheim an der Bergstrasse, Germany)

Schneider H, Hock A, Bertermann R, Radius U.
PMID: 28603878
Chemistry. 2017 Sep 07;23(50):12387-12398. doi: 10.1002/chem.201702166. Epub 2017 Jul 21.

The synthesis of mono-NHC alane adducts of the type (NHC)⋅AlH

Cite
Schneider H, Hock A, Bertermann R, et al. Reactivity of NHC Alane Adducts towards N-Heterocyclic Carbenes and Cyclic (Alkyl)(amino)carbenes: Ring Expansion, Ring Opening, and Al-H Bond Activation. Chemistry. 2017;23(50):12387-12398doi: 10.1002/chem.201702166.
Schneider, H., Hock, A., Bertermann, R., & Radius, U. (2017). Reactivity of NHC Alane Adducts towards N-Heterocyclic Carbenes and Cyclic (Alkyl)(amino)carbenes: Ring Expansion, Ring Opening, and Al-H Bond Activation. Chemistry (Weinheim an der Bergstrasse, Germany), 23(50), 12387-12398. https://doi.org/10.1002/chem.201702166
Schneider, Heidi, et al. "Reactivity of NHC Alane Adducts towards N-Heterocyclic Carbenes and Cyclic (Alkyl)(amino)carbenes: Ring Expansion, Ring Opening, and Al-H Bond Activation." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 23,50 (2017): 12387-12398. doi: https://doi.org/10.1002/chem.201702166
Schneider H, Hock A, Bertermann R, Radius U. Reactivity of NHC Alane Adducts towards N-Heterocyclic Carbenes and Cyclic (Alkyl)(amino)carbenes: Ring Expansion, Ring Opening, and Al-H Bond Activation. Chemistry. 2017 Sep 07;23(50):12387-12398. doi: 10.1002/chem.201702166. Epub 2017 Jul 21. PMID: 28603878.
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Serotoninergic Modulation of Phototactic Variability Underpins a Bet-Hedging Strategy in .

Frontiers in behavioral neuroscience

Krams IA, Krama T, Krams R, Trakimas G, Popovs S, Jõers P, Munkevics M, Elferts D, Rantala MJ, Makņa J, de Bivort BL.
PMID: 33935664
Front Behav Neurosci. 2021 Apr 16;15:659331. doi: 10.3389/fnbeh.2021.659331. eCollection 2021.

When organisms' environmental conditions vary unpredictably in time, it can be advantageous for individuals to hedge their phenotypic bets. It has been shown that a bet-hedging strategy possibly underlies the high inter-individual diversity of phototactic choice in

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Krams IA, Krama T, Krams R, et al. Serotoninergic Modulation of Phototactic Variability Underpins a Bet-Hedging Strategy in . Front Behav Neurosci. 2021;15:659331doi: 10.3389/fnbeh.2021.659331.
Krams, I. A., Krama, T., Krams, R., Trakimas, G., Popovs, S., Jõers, P., Munkevics, M., Elferts, D., Rantala, M. J., Makņa, J., & de Bivort, B. L. (2021). Serotoninergic Modulation of Phototactic Variability Underpins a Bet-Hedging Strategy in . Frontiers in behavioral neuroscience, 15659331. https://doi.org/10.3389/fnbeh.2021.659331
Krams, Indrikis A, et al. "Serotoninergic Modulation of Phototactic Variability Underpins a Bet-Hedging Strategy in ." Frontiers in behavioral neuroscience vol. 15 (2021): 659331. doi: https://doi.org/10.3389/fnbeh.2021.659331
Krams IA, Krama T, Krams R, Trakimas G, Popovs S, Jõers P, Munkevics M, Elferts D, Rantala MJ, Makņa J, de Bivort BL. Serotoninergic Modulation of Phototactic Variability Underpins a Bet-Hedging Strategy in . Front Behav Neurosci. 2021 Apr 16;15:659331. doi: 10.3389/fnbeh.2021.659331. eCollection 2021. PMID: 33935664; PMCID: PMC8085305.
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Cu-mediated .

Chemical communications (Cambridge, England)

Huang M, Tang M, Hu J, Westcott SA, Radius U, Marder TB.
PMID: 34901977
Chem Commun (Camb). 2022 Jan 04;58(3):395-398. doi: 10.1039/d1cc06144e.

A Cu-catalysed borylation of aryl alkyl sulfones was developed for the high yield synthesis of versatile arylboronic esters using a readily prepared NHC-Cu catalyst. In addition, the selective cleavage of either alkyl(C)-sulfonyl or aryl(C)-sulfonyl bonds of a cyclic sulfone

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Huang M, Tang M, Hu J, et al. Cu-mediated . Chem Commun (Camb). 2022;58(3):395-398doi: 10.1039/d1cc06144e.
Huang, M., Tang, M., Hu, J., Westcott, S. A., Radius, U., & Marder, T. B. (2022). Cu-mediated . Chemical communications (Cambridge, England), 58(3), 395-398. https://doi.org/10.1039/d1cc06144e
Huang, Mingming, et al. "Cu-mediated ." Chemical communications (Cambridge, England) vol. 58,3 (2022): 395-398. doi: https://doi.org/10.1039/d1cc06144e
Huang M, Tang M, Hu J, Westcott SA, Radius U, Marder TB. Cu-mediated . Chem Commun (Camb). 2022 Jan 04;58(3):395-398. doi: 10.1039/d1cc06144e. PMID: 34901977.
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Showing 133 to 135 of 135 entries