Results 1 to 10 of about 2,435 (258)
Repurposing Immunomodulatory Imide Drugs (IMiDs) in Neuropsychiatric and Neurodegenerative Disorders [PDF]
Neuroinflammation represents a common trait in the pathology and progression of the major psychiatric and neurodegenerative disorders. Neuropsychiatric disorders have emerged as a global crisis, affecting 1 in 4 people, while neurological disorders are the second leading cause of death in the elderly population worldwide (WHO, 2001;GBD 2016 Neurology ...
Yoo Jin Jung +9 more
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Phosphorescent perylene imides [PDF]
Asymmetrically substituted perylene imide derivatives PIa and PIx display phosphorescence in glassy matrices at 77 K. The lifetime is 49.0 ms for PIa and 13.5 ms for PIx. The triplet energy is 1.79 eV for PIa and 1.68 eV for PIx as confirmed by sensitization experiments of the C(60) triplet.
Ventura +7 more
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The imide tautomer of sulfasalazine [PDF]
The title compound, 5-[4-[(2-pyridylideneamino)sulfonyl]phenyldiazenyl]salicylic acid, C(18)H(14)N(4)O(5)S, crystallizes as the imide tautomer in the monoclinic space group P2(1)/c. In addition to an intramolecular O-H.O hydrogen bond, intermolecular O-H.O interactions link adjacent molecules into helices, which are connected by pairwise N-H.N ...
Blake, A.J. +5 more
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Citation: 'imides' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.I02948 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
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Exploring the Azabenzannulation of Benzothioxanthene Imide
We report herein the synthesis and characterization of azabenzannulated benzothioxanthene imides (BTIs) functionalized with various appended aromatic units. This new class of polycyclic aromatic hydrocarbons is prepared via a straightforward and efficient synthetic strategy that involves a visible-light-mediated photocyclization of imines.
David, Arthur H. G. +8 more
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Citation: 'amine imides' in the IUPAC Compendium of Chemical Terminology, 3rd ed.; International Union of Pure and Applied Chemistry; 2006. Online version 3.0.1, 2019. 10.1351/goldbook.A00271 • License: The IUPAC Gold Book is licensed under Creative Commons Attribution-ShareAlike CC BY-SA 4.0 International for individual terms.
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Ring-opening decarbonylative C(sp<sup>3</sup>)-C(sp<sup>3</sup>) cross-electrophile coupling of cyclic imides with unactivated alkyl chlorides. [PDF]
Lentelink NJ +3 more
europepmc +1 more source
Anion Component Engineering of Spontaneous Perovskite Passivators for Energy Alignment Modulations in Perovskite Solar Cells. [PDF]
Nishimura N, Tachibana H, Murakami TN.
europepmc +1 more source
Reversible, Polymeric Complexation of Therapeutic Peptides Using Esterification. [PDF]
Gourishankar AS +5 more
europepmc +1 more source
Anti-Inflammatory Activity of Cyclic Imide Derivatives. [PDF]
Redzicka A, Tylińska B, Wójcicka A.
europepmc +1 more source

