These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Synthesis of octyl arabinofuranosides as substrates for mycobacterial arabinosyltransferases.
    Author: Han J, Gadikota RR, McCarren PR, Lowary TL.
    Journal: Carbohydr Res; 2003 Mar 28; 338(7):581-8. PubMed ID: 12644370.
    Abstract:
    A panel of octyl oligosaccharides comprised of arabinofuranose rings have been synthesized via efficient and readily scaleable routes. The key glycosylation reactions involved the coupling of octyl glycoside acceptors with the appropriate thioglycosides using N-iodosuccinimide and silver triflate activation. These syntheses were undertaken to provide substrates suitable for use in assays of mycobacterial arabinosyltransferases.
    [Abstract] [Full Text] [Related] [New Search]