Organocatalytic asymmertric reactions : aminoxylation, Michael and their tandem reactions

A 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.

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Main Author: Chua, Pei Juan
Other Authors: Zhong Guofu
Format: Theses and Dissertations
Language:English
Published: 2011
Subjects:
Online Access:https://hdl.handle.net/10356/46227
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-462272023-02-28T23:52:48Z Organocatalytic asymmertric reactions : aminoxylation, Michael and their tandem reactions Chua, Pei Juan Zhong Guofu School of Physical and Mathematical Sciences DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis A 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. DOCTOR OF PHILOSOPHY (SPMS) 2011-07-08T02:40:28Z 2011-07-08T02:40:28Z 2011 2011 Thesis Chua, P. J. (2011). Organocatalytic asymmertric reactions : aminoxylation, Michael and their tandem reactions. Doctoral thesis, Nanyang Technological University, Singapore. https://hdl.handle.net/10356/46227 10.32657/10356/46227 en 163 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::Chemistry::Organic chemistry::Organic synthesis
spellingShingle DRNTU::Science::Chemistry::Organic chemistry::Organic synthesis
Chua, Pei Juan
Organocatalytic asymmertric reactions : aminoxylation, Michael and their tandem reactions
description A 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.
author2 Zhong Guofu
author_facet Zhong Guofu
Chua, Pei Juan
format Theses and Dissertations
author Chua, Pei Juan
author_sort Chua, Pei Juan
title Organocatalytic asymmertric reactions : aminoxylation, Michael and their tandem reactions
title_short Organocatalytic asymmertric reactions : aminoxylation, Michael and their tandem reactions
title_full Organocatalytic asymmertric reactions : aminoxylation, Michael and their tandem reactions
title_fullStr Organocatalytic asymmertric reactions : aminoxylation, Michael and their tandem reactions
title_full_unstemmed Organocatalytic asymmertric reactions : aminoxylation, Michael and their tandem reactions
title_sort organocatalytic asymmertric reactions : aminoxylation, michael and their tandem reactions
publishDate 2011
url https://hdl.handle.net/10356/46227
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