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Aziridines

"Aziridines" 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
Saturated azacyclopropane compounds. They include compounds with substitutions on CARBON or NITROGEN atoms.


expand / collapse Publications
This graph shows the total number of publications written about "Aziridines" by people in this website by year, and whether "Aziridines" was a major or minor topic of these publications.
Below are the most recent publications written about "Aziridines" by people in Profiles.
  1. Photorearrangement of [8]-2,6-Pyridinophane N-Oxide. J Am Chem Soc. 2020 12 09; 142(49):20717-20724.
    View in: PubMed
  2. Chemoablation in Urothelial Carcinoma: A Systematic Review and Future Perspectives. Urology. 2020 10; 144:28-37.
    View in: PubMed
  3. Systematic identification of engineered methionines and oxaziridines for efficient, stable, and site-specific antibody bioconjugation. Proc Natl Acad Sci U S A. 2020 03 17; 117(11):5733-5740.
    View in: PubMed
  4. Efficient Prodrug Activator Gene Therapy by Retroviral Replicating Vectors Prolongs Survival in an Immune-Competent Intracerebral Glioma Model. Int J Mol Sci. 2020 Feb 20; 21(4).
    View in: PubMed
  5. Design, Synthesis, and Biological Investigation of Epothilone B Analogues Featuring Lactone, Lactam, and Carbocyclic Macrocycles, Epoxide, Aziridine, and 1,1-Difluorocyclopropane and Other Fluorine Residues. J Org Chem. 2020 03 06; 85(5):2865-2917.
    View in: PubMed
  6. Expanding the Scope of Electrophiles Capable of Targeting K-Ras Oncogenes. Biochemistry. 2017 06 27; 56(25):3178-3183.
    View in: PubMed
  7. 12,13-Aziridinyl Epothilones. Stereoselective Synthesis of Trisubstituted Olefinic Bonds from Methyl Ketones and Heteroaromatic Phosphonates and Design, Synthesis, and Biological Evaluation of Potent Antitumor Agents. J Am Chem Soc. 2017 05 31; 139(21):7318-7334.
    View in: PubMed
  8. Redox-based reagents for chemoselective methionine bioconjugation. Science. 2017 02 10; 355(6325):597-602.
    View in: PubMed
  9. Scalable antifouling reverse osmosis membranes utilizing perfluorophenyl azide photochemistry. Macromol Rapid Commun. 2014 Sep; 35(17):1528-33.
    View in: PubMed
  10. Stereochemical lability of azatitanacyclopropanes: dynamic kinetic resolution in reductive cross-coupling reactions with allylic alcohols. Chem Commun (Camb). 2013 Oct 09; 49(78):8857-9.
    View in: PubMed