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    Intramolecular monomer-on-monomer (MoM) mitsunobu cyclization for the synthesis of benzofused thiadiazepine-dioxides

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    Issue Date
    2012-06-14
    Author
    Maity, Pradip K.
    Kainz, Quirin M.
    Faisal, Saqib
    Rolfe, Alan
    Samarakoon, Thiwanka Bandara
    Basha, Fatima Z.
    Reiser, Oliver
    Hanson, Paul R.
    Publisher
    Royal Society of Chemistry
    Type
    Article
    Article Version
    Scholarly/refereed, author accepted manuscript
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    Abstract
    The utilization of a monomer-on-monomer (MoM) intramolecular Mitsunobu cyclization reaction employing norbornenyl-tagged (Nb-tagged) reagents is reported for the synthesis of benzofused thiadiazepine-dioxides. Facile purification was achieved via ring-opening metathesis (ROM) polymerization initiated by one of three metathesis catalyst methods: (i) free metathesis catalyst, (ii) surface-initiated catalyst-armed silica, or (iii) surface-initiated catalyst-armed Co/C magnetic nanoparticles.
    URI
    http://hdl.handle.net/1808/23222
    DOI
    https://doi.org/10.1039/c1cc14807a
    Collections
    • Chemistry Scholarly Works [553]
    Citation
    Maity, Pradip K., Quirin M. Kainz, Saqib Faisal, Alan Rolfe, Thiwanka. B. Samarakoon, Fatima Z. Basha, Oliver Reiser, and Paul R. Hanson. "Intramolecular Monomer-on-monomer (MoM) Mitsunobu Cyclization for the Synthesis of Benzofused Thiadiazepine-dioxides." Chemical Communications 47.46 (2011): 12524.

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    Contact KU ScholarWorks
    785-864-8983
    KU Libraries
    1425 Jayhawk Blvd
    Lawrence, KS 66045
    785-864-8983

    KU Libraries
    1425 Jayhawk Blvd
    Lawrence, KS 66045
    Image Credits
     

     

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