Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12202/4782
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dc.contributor.advisorCamara, James-
dc.contributor.authorSchiff, Elliot-
dc.date.accessioned2019-10-29T15:24:20Z-
dc.date.available2019-10-29T15:24:20Z-
dc.date.issued2019-07-
dc.identifier.citationSchiff, Elliot. (July 2019). Methods of Determining Enantiomeric Excess of Secondary Phosphines. Thesis Submitted in Partial Fulfillment of the Requirements of the Jay and Jeanie Schottenstein Honors Program. Yeshiva College, Yeshiva Universityen_US
dc.identifier.urihttps://hdl.handle.net/20.500.12202/4782-
dc.descriptionSenior thesisen_US
dc.description.abstractAbstract Secondary Phosphines can be directly synthesized through P-C cross-coupling.1 However, there is no published method for determining the enantiomeric excess of secondary phosphines. Development of a method to measure the enantiomeric excess of secondary phosphines is crucial for the ongoing utility of these compounds in pharmaceutical and industrial applications. Using phenyl(xylyl) phosphine as a test case, a series of chiral shift reagents were employed to find a method of determining the enantiomeric excess. Following this, several chiral derivatization agents were employed to convert phenyl(xylyl) phosphine into a pair of identifiable diastereomers to allow measuring the enantiomeric excess. The most promising option was R-menthyl-chloroformate, although the conversion percentage did not exceed 30%.en_US
dc.description.sponsorshipThe Jay and Jeanie Schottenstein Honors Programen_US
dc.language.isoen_USen_US
dc.publisherNY: Yeshiva College. Yeshiva University.en_US
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.subjectSenior honors thesisen_US
dc.subjectSecondary phosphines -- Enantiomeric excessen_US
dc.titleMethods of Determining Enantiomeric Excess of Secondary Phosphines.en_US
dc.typeThesisen_US
Appears in Collections:Jay and Jeanie Schottenstein Honors Student Theses

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