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dc.contributor.advisorMaleczka, Robert E., Jr.
dc.contributor.authorToskey, Elli A.
dc.date.accessioned2008-09-25T19:18:34Z
dc.date.available2008-09-25T19:18:34Z
dc.date.issued2008-09-25T19:18:34Z
dc.identifier.urihttp://hdl.handle.net/10920/6058
dc.description.abstractA method has been devised to cross couple acid chlorides using tributyltin fluoride (BU3SnF) and polymethylhydrosiloxane (PMHS) in Stille coupling. This method employs Bu3SnF and PMHS as an in situ tin hydride source while performing the experiment in one pot. These techniques avoid the toxic tin intermediates commonly associated with Stille couplings.en
dc.language.isoen_USen
dc.relation.ispartofseriesSenior Individualized Projects. Chemistry.en
dc.rightsU.S. copyright laws protect this material. Commercial use or distribution of this material is not permitted without prior written permission of the copyright holder.
dc.subject.lcshChlorides
dc.titleOne-pot hydrostannation/Stille couplings of acid chlorides using tributyltin flouride and polymethylhydrosiloxane as an in situ tin hydride sourceen
dc.typeThesisen


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  • Chemistry Senior Individualized Projects [827]
    This collection includes Senior Individualized Projects (SIP's) completed in the Chemistry Department. Abstracts are generally available to the public, but PDF files are available only to current Kalamazoo College students, faculty, and staff.

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