Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/46316
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dc.contributor.authorZhu, Di
dc.date.accessioned2011-11-30T03:13:42Z
dc.date.available2011-11-30T03:13:42Z
dc.date.copyright2011en_US
dc.date.issued2011
dc.identifier.urihttp://hdl.handle.net/10356/46316
dc.description.abstractIn 2000, List and co-workers firstly reported that L-proline was an effective asymmetric catalyst for the direct aldol reaction between unmodified acetone an a variety of aldehydes, with yields and enantioselectivities from moderate to good. This discovery has initiated the explosive growth of research activities in organic chemistry. Now asymmetric organo-catalysis in which small chiral organic molecules act as catalytically active species, emerged as powerful synthetic tool and are complementary to transition metal based catalysis and biocatalysis in asymmetric synthesis.en_US
dc.format.extent83 p.en_US
dc.language.isoenen_US
dc.subjectDRNTU::Scienceen_US
dc.titleHighly stereoselective synthesis of tetrahydro-1,2-oxazines and bicyclic isoxazolidines from nitroso benzenes and 5-alkenylaldehydesen_US
dc.typeThesis
dc.contributor.supervisorZhong Guofuen_US
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.description.degree​Master of Scienceen_US
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