STEREOSELECTIVITY AND REGIOSELECTIVITY<br />IN ORGANIC CHEMISTRY: NOVEL SYSTEMS AND<br />APPLICATIONS

Molecular recognition has become a very important field of research in chemistry during the last decades. This<br />chemical phenomenon is responsible for all processes occurring in biology and asymmetric synthesis is based<br />upon the capability of molecules or substrates to recognise...

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Main Author: Legrand, Sacha
Language:ENG
Published: 2006
Subjects:
NMR
Online Access:http://tel.archives-ouvertes.fr/tel-00080096
http://tel.archives-ouvertes.fr/docs/00/08/00/96/PDF/THESIS.pdf
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spelling ndltd-CCSD-oai-tel.archives-ouvertes.fr-tel-000800962013-01-07T18:54:47Z http://tel.archives-ouvertes.fr/tel-00080096 http://tel.archives-ouvertes.fr/docs/00/08/00/96/PDF/THESIS.pdf STEREOSELECTIVITY AND REGIOSELECTIVITY<br />IN ORGANIC CHEMISTRY: NOVEL SYSTEMS AND<br />APPLICATIONS Legrand, Sacha [CHIM:OTHE] Chemical Sciences/Other aldol reaction Argyrotaenia sphaleropa Hylobius abietis methyl benzoic esters molecularly<br />imprinted polymer molecular recognition NMR pheromones regioselectivity stereoselectivity TADDOL Molecular recognition has become a very important field of research in chemistry during the last decades. This<br />chemical phenomenon is responsible for all processes occurring in biology and asymmetric synthesis is based<br />upon the capability of molecules or substrates to recognise each other in a selective manner. In this thesis, the<br />design, preparation and evaluation of a series of new synthetic receptors has been described. The importance of<br />regioselectivity and stereoselectivity in molecular recognition has also been underlined with two different<br />biological examples.<br />The capability of host molecules, derived from (+)-tartaric acid, to accommodate various guests in a selective<br />manner was demonstrated using 1H-NMR spectroscopy (paper I). These host molecules, known as TADDOLs,<br />enantioselectively recognised the valuable chiral alcohols glycidol and menthol. Macromolecular receptors, i.e.<br />molecularly imprinted polymers (MIPs), were also prepared in order to catalyse the aldol reaction between either<br />(R)- or (S)-camphor and benzaldehyde (paper II). With the help of analytical methods, it was demonstrated that<br />the MIPs interacted in a selective manner with the enantiomers of camphor. Moreover, these MIPs enhanced<br />significantly the rate of the aldol condensation mentioned above.<br />Regarding biological systems, various regioisomeric analogues of benzoic acid have been tested as antifeedants<br />against the pine weevil Hylobius abietis (paper III and IV). The regioisomers studied displayed very different<br />antifeedant activities. The significance of stereoisomerism on pheromone function has been shown in the<br />preparation of lures for the control of the insect pest Argyrotaenia sphaleropa (paper V). It was demonstrated that<br />male leafrollers could be caught by a lure containing components of the female sex pheromone gland. 2006-03-02 ENG PhD thesis
collection NDLTD
language ENG
sources NDLTD
topic [CHIM:OTHE] Chemical Sciences/Other
aldol reaction
Argyrotaenia sphaleropa
Hylobius abietis
methyl benzoic esters
molecularly<br />imprinted polymer
molecular recognition
NMR
pheromones
regioselectivity
stereoselectivity
TADDOL
spellingShingle [CHIM:OTHE] Chemical Sciences/Other
aldol reaction
Argyrotaenia sphaleropa
Hylobius abietis
methyl benzoic esters
molecularly<br />imprinted polymer
molecular recognition
NMR
pheromones
regioselectivity
stereoselectivity
TADDOL
Legrand, Sacha
STEREOSELECTIVITY AND REGIOSELECTIVITY<br />IN ORGANIC CHEMISTRY: NOVEL SYSTEMS AND<br />APPLICATIONS
description Molecular recognition has become a very important field of research in chemistry during the last decades. This<br />chemical phenomenon is responsible for all processes occurring in biology and asymmetric synthesis is based<br />upon the capability of molecules or substrates to recognise each other in a selective manner. In this thesis, the<br />design, preparation and evaluation of a series of new synthetic receptors has been described. The importance of<br />regioselectivity and stereoselectivity in molecular recognition has also been underlined with two different<br />biological examples.<br />The capability of host molecules, derived from (+)-tartaric acid, to accommodate various guests in a selective<br />manner was demonstrated using 1H-NMR spectroscopy (paper I). These host molecules, known as TADDOLs,<br />enantioselectively recognised the valuable chiral alcohols glycidol and menthol. Macromolecular receptors, i.e.<br />molecularly imprinted polymers (MIPs), were also prepared in order to catalyse the aldol reaction between either<br />(R)- or (S)-camphor and benzaldehyde (paper II). With the help of analytical methods, it was demonstrated that<br />the MIPs interacted in a selective manner with the enantiomers of camphor. Moreover, these MIPs enhanced<br />significantly the rate of the aldol condensation mentioned above.<br />Regarding biological systems, various regioisomeric analogues of benzoic acid have been tested as antifeedants<br />against the pine weevil Hylobius abietis (paper III and IV). The regioisomers studied displayed very different<br />antifeedant activities. The significance of stereoisomerism on pheromone function has been shown in the<br />preparation of lures for the control of the insect pest Argyrotaenia sphaleropa (paper V). It was demonstrated that<br />male leafrollers could be caught by a lure containing components of the female sex pheromone gland.
author Legrand, Sacha
author_facet Legrand, Sacha
author_sort Legrand, Sacha
title STEREOSELECTIVITY AND REGIOSELECTIVITY<br />IN ORGANIC CHEMISTRY: NOVEL SYSTEMS AND<br />APPLICATIONS
title_short STEREOSELECTIVITY AND REGIOSELECTIVITY<br />IN ORGANIC CHEMISTRY: NOVEL SYSTEMS AND<br />APPLICATIONS
title_full STEREOSELECTIVITY AND REGIOSELECTIVITY<br />IN ORGANIC CHEMISTRY: NOVEL SYSTEMS AND<br />APPLICATIONS
title_fullStr STEREOSELECTIVITY AND REGIOSELECTIVITY<br />IN ORGANIC CHEMISTRY: NOVEL SYSTEMS AND<br />APPLICATIONS
title_full_unstemmed STEREOSELECTIVITY AND REGIOSELECTIVITY<br />IN ORGANIC CHEMISTRY: NOVEL SYSTEMS AND<br />APPLICATIONS
title_sort stereoselectivity and regioselectivity<br />in organic chemistry: novel systems and<br />applications
publishDate 2006
url http://tel.archives-ouvertes.fr/tel-00080096
http://tel.archives-ouvertes.fr/docs/00/08/00/96/PDF/THESIS.pdf
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