dc.contributor.authorChua, Pei Juan
dc.date.accessioned2011-07-08T02:40:28Z
dc.date.accessioned2017-07-23T08:43:24Z
dc.date.available2011-07-08T02:40:28Z
dc.date.available2017-07-23T08:43:24Z
dc.date.copyright2011en_US
dc.date.issued2011
dc.identifier.citationChua, P. J. (2011). Organocatalytic asymmertric reactions : aminoxylation, Michael and their tandem reactions. Doctoral thesis, Nanyang Technological University, Singapore.
dc.identifier.urihttp://hdl.handle.net/10356/46227
dc.description.abstractA highly enantioselectve L-thiaprolnie-catalysed a-aminoxylation of aldehydes in the presence of water and tertrabutylammonium bromide followed by in situ reduction to afford the respective a-aminoxy alcohols in good to high yields and excellent enantioselectivities was first developed.en_US
dc.format.extent163 p.en_US
dc.language.isoenen_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistry::Organic synthesisen_US
dc.titleOrganocatalytic asymmertric reactions : aminoxylation, Michael and their tandem reactionsen_US
dc.typeThesis
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.contributor.supervisorZhong Guofuen_US
dc.description.degreeDOCTOR OF PHILOSOPHY (SPMS)en_US


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