Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/142898
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dc.contributor.authorTay, Wee Shanen_US
dc.date.accessioned2020-07-07T06:45:51Z-
dc.date.available2020-07-07T06:45:51Z-
dc.date.issued2020-
dc.identifier.citationTay, W. S (2020). Developing the catalytic asymmetric hydroarsination reaction. Doctoral thesis, Nanyang Technological University, Singapore.en_US
dc.identifier.urihttps://hdl.handle.net/10356/142898-
dc.description.abstractThe asymmetric hydroarsination reaction is arguably the most atom-economical and efficient manner to produce chiral arsines with high enantiopurities. Although various catalysts have been developed for the analogous hydrophosphination reaction, none have been effective for the hydroarsination reaction thus far. Herein, the development of organometallic (Pd- and Ni- based) and organic (phosphine-based) catalytic systems for the hydroarsination reaction is discussed. Mechanistic investigations reveal that arsines were not direct substitutes of phosphines in this instance. Consequently, arsines were applied in several novel applications such as in deuteration, decomplexation and as a directing group. The relevance of these developments to general synthetic chemistry is also outlined.en_US
dc.language.isoenen_US
dc.publisherNanyang Technological Universityen_US
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC 4.0).en_US
dc.subjectScience::Chemistry::Organic chemistry::Organometallic compoundsen_US
dc.titleDeveloping the catalytic asymmetric hydroarsination reactionen_US
dc.typeThesis-Doctor of Philosophyen_US
dc.contributor.supervisorLeung Pak Hingen_US
dc.contributor.supervisorPullarkat Appukuttan Sumoden_US
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.description.degreeDoctor of Philosophyen_US
dc.identifier.doi10.32657/10356/142898-
dc.contributor.supervisoremailpakhing@ntu.edu.sg, Sumod@ntu.edu.sgen_US
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