imine【有化】 - PMC

Juliana V. Kuznetsova, Varvara T. Tkachenko, Lada M. Petrovskaya, Maria E. Filkina, Dmitry E. Shybanov, Yuri K. Grishin, Vitaly A. Roznyatovsky, Viktor A. Tafeenko, Anna S. Pestretsova, Vera A. Yakovleva, Vadim S. Pokrovsky, Maxim E. Kukushkin, Elena K. Beloglazkina

Int J Mol Sci. 2024 Jan; 25(1): 18. Published online 2023 Dec 19. doi: 10.3390/ijms25010018

PMCID:: PMC10778941

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N-tert-Butanesulfinyl imines in the asymmetric synthesis of nitrogen-containing heterocycles

Joseane A Mendes, Paulo R R Costa, Miguel Yus, Francisco Foubelo, Camilla D Buarque

Beilstein J Org Chem. 2021; 17: 1096–1140. Published online 2021 May 12. doi: 10.3762/bjoc.17.86

PMCID:: PMC8144919

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A new look at imines and their mixture with PC₇₁BM for organic, flexible photovoltaics

Krzysztof A. Bogdanowicz, Sebastian Lalik, Paulina Ratajczyk, Andrzej Katrusiak, Piotr Krysiak, Agnieszka I. Pawłowska, Monika Marzec, Agnieszka Iwan

Sci Rep. 2023; 13: 13240. Published online 2023 Aug 14. doi: 10.1038/s41598-023-38978-x

Correction in:: Sci Rep. 2023; 13: 15150.

PMCID:: PMC10425360

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A Theoretical Investigation of Novel Sila- and Germa-Spirocyclic Imines and Their Relevance for Electron-Transporting Materials and Drug Discovery

Marwan Dakkouri

Molecules. 2023 Sep; 28(17): 6298. Published online 2023 Aug 28. doi: 10.3390/molecules28176298

PMCID:: PMC10489060

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Visible-Light, Iodine-Promoted Formation of N-Sulfonyl Imines and N-Alkylsulfonamides from Aldehydes and Hypervalent Iodine Reagents

Megan D. Hopkins, Zachary C. Brandeburg, Andrew J. Hanson, Angus A. Lamar

Molecules. 2018 Aug; 23(8): 1838. Published online 2018 Jul 24. doi: 10.3390/molecules23081838

PMCID:: PMC6222766

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Intermolecular 2+2 imine-olefin photocycloadditions enabled by Cu(I)-alkene MLCT

Daniel M. Flores, Michael L. Neville, Valerie A. Schmidt

Nat Commun. 2022; 13: 2764. Published online 2022 May 19. doi: 10.1038/s41467-022-30393-6

PMCID:: PMC9120151

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Asymmetric Allylboration of Acyl Imines Catalyzed by Chiral Diols

Sha Lou, Philip N. Moquist, Scott E. Schaus

J Am Chem Soc. Author manuscript; available in PMC 2009 Feb 10.

Published in final edited form as: J Am Chem Soc. 2007 Dec 12; 129(49): 15398–15404. Published online 2007 Nov 17. doi: 10.1021/ja075204v

PMCID:: PMC2638762

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Imine- and Amine-Type Macrocycles Derived from Chiral Diamines and Aromatic Dialdehydes

Jerzy Lisowski

Molecules. 2022 Jul; 27(13): 4097. Published online 2022 Jun 25. doi: 10.3390/molecules27134097

PMCID:: PMC9267964

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Systematic Evaluation of Imine‐Reducing Enzymes: Common Principles in Imine Reductases, β‐Hydroxy Acid Dehydrogenases, and Short‐Chain Dehydrogenases/ Reductases

Peter Stockinger, Sebastian Roth, Prof. Dr. Michael Müller, Prof. Dr. Jürgen Pleiss

Chembiochem. 2020 Sep 14; 21(18): 2689–2695. Published online 2020 May 29. doi: 10.1002/cbic.202000213

PMCID:: PMC7540600

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Catalytic Asymmetric Umpolung Reactions of Imines

Yongwei Wu, Lin Hu, Zhe Li, Li Deng

Nature. Author manuscript; available in PMC 2016 Jan 23.

Published in final edited form as: Nature. 2015 Jul 23; 523(7561): 445–450. doi: 10.1038/nature14617

PMCID:: PMC4513368

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Asymmetric Reactions of N-Phosphonyl/Phosphoryl Imines

Devalina Ray, Suman Majee, Ram Naresh Yadav, Bimal Krishna Banik

Molecules. 2023 Apr; 28(8): 3524. Published online 2023 Apr 17. doi: 10.3390/molecules28083524

PMCID:: PMC10143947

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Opportunities Offered by Chiral η⁶-Arene/N-Arylsulfonyl-diamine-Ru^II Catalysts in the Asymmetric Transfer Hydrogenation of Ketones and Imines

Jiří Václavík, Petr Kačer, Marek Kuzma, Libor Červený

Molecules. 2011 Jul; 16(7): 5460–5495. Published online 2011 Jun 28. doi: 10.3390/molecules16075460

PMCID:: PMC6264677

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A Plausible Mechanism for the Iridium-Catalyzed Hydrogenation of a Bulky N-Aryl Imine in the (S)-Metolachlor Process

Amanda L. Kwan, Robert H. Morris

Molecules. 2022 Aug; 27(16): 5106. Published online 2022 Aug 11. doi: 10.3390/molecules27165106

PMCID:: PMC9414898

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Biological Evaluation and Mechanistic Studies of Quinolin-(1H)-Imines as a New Chemotype against Leishmaniasis

Ana Georgina Gomes-Alves, Margarida Duarte, Tânia Cruz, Helena Castro, Francisca Lopes, Rui Moreira, Ana S. Ressurreição, Ana M. Tomás

Antimicrob Agents Chemother. 2021 Jul; 65(7): e01513-20. Prepublished online 2021 Apr 26. Published online 2021 Jun 17. doi: 10.1128/AAC.01513-20

PMCID:: PMC8218623

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Stereoselective Reduction of Imines with Trichlorosilane Using Solid-Supported Chiral Picolinamides

Sílvia D. Fernandes, Riccardo Porta, Pedro C. Barrulas, Alessandra Puglisi, Anthony J. Burke, Maurizio Benaglia

Molecules. 2016 Sep; 21(9): 1182. Published online 2016 Sep 6. doi: 10.3390/molecules21091182

PMCID:: PMC6274114

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Fabrication, DFT Calculation, and Molecular Docking of Two Fe(III) Imine Chelates as Anti-COVID-19 and Pharmaceutical Drug Candidate

Hany M. Abd El-Lateef, Mai M. Khalaf, Mohamed R. Shehata, Ahmed M. Abu-Dief

Int J Mol Sci. 2022 Apr; 23(7): 3994. Published online 2022 Apr 3. doi: 10.3390/ijms23073994

PMCID:: PMC8999679

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Fig. 1Azides derived synthons and transition metal imine complexes.

(A) Transition metal–catalyzed C–N bond formation from azides. (B) Isolated transition metal imine complexes.

In situ generation of N-unsubstituted imines from alkyl azides and their applications for imine transfer via copper catalysis

Sci Adv. 2017 Aug;3(8):e1700826.
Fig. 2The construction of C–N bonds through imine transfer reactions using azides as nitrogen source.

(A) Modulating ligands enables imine transfer reactions using azides. (B) This work.

In situ generation of N-unsubstituted imines from alkyl azides and their applications for imine transfer via copper catalysis

Sci Adv. 2017 Aug;3(8):e1700826.
Figure 6

Reaction coordinate diagram for the investigated hydride transfers in DCE, with the acetaldehyde (red), imine 1 (purple), acetone (orange), imine 2 (blue), formaldehyde (pink), and imine 3 (green) represented in the six reaction pathways. Imine 1 refers to Z-methylethylideneimine (acetaldehyde + methylamine), imine 2 refers to N-methyl-2-propylideneimine (acetone + methylamine), and imine 3 refers to N-methylmethanimine (formaldehyde + methylamine).

Density Functional Theory Study on the Selective Reductive Amination of Aldehydes and Ketones over Their Reductions to Alcohols Using Sodium Triacetoxyborohydride

ACS Omega. 2022 Aug 30;7(34):30554-30564.
SCHEME 4.

A hypothetical kinetic mechanism of ecQueF-imine complex dissociation induced by preQ₀ is shown. E is the free enzyme. The enzyme-bound preQ₀ and imine are indicated by subscript. E∼imine indicates a preassociated complex of ecQueF with imine intermediate. The model is adapted from literature ().

Evidence of a sequestered imine intermediate during reduction of nitrile to amine by the nitrile reductase QueF from Escherichia coli

J Biol Chem. 2018 Mar 9;293(10):3720-3733.