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Imines

"Imines" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

expand / collapse MeSH information
Organic compounds containing a carbon-nitrogen double bond where a NITROGEN atom can be attached to HYDROGEN or an alkyl or aryl group.


expand / collapse Publications
This graph shows the total number of publications written about "Imines" by people in this website by year, and whether "Imines" was a major or minor topic of these publications.
Below are the most recent publications written about "Imines" by people in Profiles.
  1. Insights into the Biological Activity and Bio-Interaction Properties of Nanoscale Imine-Based 2D and 3D Covalent Organic Frameworks. Adv Sci (Weinh). 2024 Nov; 11(44):e2407391.
    View in: PubMed
  2. The Cyclic Imine Core Common to the Marine Macrocyclic Toxins Is Sufficient to Dictate Nicotinic Acetylcholine Receptor Antagonism. Mar Drugs. 2024 Mar 27; 22(4).
    View in: PubMed
  3. Bioactive Bromotyrosine Alkaloids from the Bahamian Marine Sponge Aiolochroia crassa. Dimerization and Oxidative Motifs. J Org Chem. 2022 10 07; 87(19):12831-12843.
    View in: PubMed
  4. Metabolomic Evaluation of N-Acetyl-p-Benzoquinone Imine Protein Adduct Formation with Therapeutic Acetaminophen Administration: Sex-based Physiologic Differences. J Med Toxicol. 2022 10; 18(4):297-310.
    View in: PubMed
  5. Intermolecular 2+2 imine-olefin photocycloadditions enabled by Cu(I)-alkene MLCT. Nat Commun. 2022 05 19; 13(1):2764.
    View in: PubMed
  6. Asymmetric Organocatalysis Enables Rapid Assembly of Portimine Precursor Chains. Org Lett. 2022 04 15; 24(14):2607-2612.
    View in: PubMed
  7. 1,3-Asymmetric Induction in Diastereoselective Allylations of Chiral N-Tosyl Imines. J Org Chem. 2022 03 04; 87(5):2773-2778.
    View in: PubMed
  8. Protein Modification at Tyrosine with Iminoxyl Radicals. J Am Chem Soc. 2021 12 01; 143(47):19844-19855.
    View in: PubMed
  9. Mechanistic Investigation of Castagnoli-Cushman Multicomponent Reactions Leading to a Three-Component Synthesis of Dihydroisoquinolones. J Org Chem. 2021 09 03; 86(17):11599-11607.
    View in: PubMed
  10. Peroxidasin-mediated bromine enrichment of basement membranes. Proc Natl Acad Sci U S A. 2020 07 07; 117(27):15827-15836.
    View in: PubMed