Highly stereoselective synthesis of tetrahydro-1,2-oxazines and bicyclic isoxazolidines from nitroso benzenes and 5-alkenylaldehydes

In 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 resea...

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Main Author:	Zhu, Di
Other Authors:	Zhong Guofu
Format:	Theses and Dissertations
Language:	English
Published:	2011
Subjects:	DRNTU::Science
Online Access:	http://hdl.handle.net/10356/46316
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Institution:	Nanyang Technological University
Language:	English

id	sg-ntu-dr.10356-46316
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spelling	sg-ntu-dr.10356-463162023-02-28T23:53:00Z Highly stereoselective synthesis of tetrahydro-1,2-oxazines and bicyclic isoxazolidines from nitroso benzenes and 5-alkenylaldehydes Zhu, Di Zhong Guofu School of Physical and Mathematical Sciences DRNTU::Science In 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. Master of Science 2011-11-30T03:13:42Z 2011-11-30T03:13:42Z 2011 2011 Thesis http://hdl.handle.net/10356/46316 en 83 p. application/pdf
institution	Nanyang Technological University
building	NTU Library
continent	Asia
country	Singapore Singapore
content_provider	NTU Library
collection	DR-NTU
language	English
topic	DRNTU::Science
spellingShingle	DRNTU::Science Zhu, Di Highly stereoselective synthesis of tetrahydro-1,2-oxazines and bicyclic isoxazolidines from nitroso benzenes and 5-alkenylaldehydes
description	In 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.
author2	Zhong Guofu
author_facet	Zhong Guofu Zhu, Di
format	Theses and Dissertations
author	Zhu, Di
author_sort	Zhu, Di
title	Highly stereoselective synthesis of tetrahydro-1,2-oxazines and bicyclic isoxazolidines from nitroso benzenes and 5-alkenylaldehydes
title_short	Highly stereoselective synthesis of tetrahydro-1,2-oxazines and bicyclic isoxazolidines from nitroso benzenes and 5-alkenylaldehydes
title_full	Highly stereoselective synthesis of tetrahydro-1,2-oxazines and bicyclic isoxazolidines from nitroso benzenes and 5-alkenylaldehydes
title_fullStr	Highly stereoselective synthesis of tetrahydro-1,2-oxazines and bicyclic isoxazolidines from nitroso benzenes and 5-alkenylaldehydes
title_full_unstemmed	Highly stereoselective synthesis of tetrahydro-1,2-oxazines and bicyclic isoxazolidines from nitroso benzenes and 5-alkenylaldehydes
title_sort	highly stereoselective synthesis of tetrahydro-1,2-oxazines and bicyclic isoxazolidines from nitroso benzenes and 5-alkenylaldehydes
publishDate	2011
url	http://hdl.handle.net/10356/46316
_version_	1759856989582655488

Highly stereoselective synthesis of tetrahydro-1,2-oxazines and bicyclic isoxazolidines from nitroso benzenes and 5-alkenylaldehydes

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