dc.contributor.advisor | Camara, James | |
dc.contributor.author | Schiff, Elliot | |
dc.date.accessioned | 2019-10-29T15:24:20Z | |
dc.date.available | 2019-10-29T15:24:20Z | |
dc.date.issued | 2019-07 | |
dc.identifier.citation | Schiff, 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 University | en_US |
dc.identifier.uri | https://hdl.handle.net/20.500.12202/4782 | |
dc.description | Senior thesis | en_US |
dc.description.abstract | Abstract
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.sponsorship | The Jay and Jeanie Schottenstein Honors Program | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | NY: Yeshiva College. Yeshiva University. | en_US |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/us/ | * |
dc.subject | Senior honors thesis | en_US |
dc.subject | Secondary phosphines -- Enantiomeric excess | en_US |
dc.title | Methods of Determining Enantiomeric Excess of Secondary Phosphines. | en_US |
dc.type | Thesis | en_US |