Computational analysis of the enantioselectivity of diels-alder reactions involving chiral cationic oxazaborolidinium catalyst / Nasr Y.M. Omar

This thesis is divided into six chapters. In the first chapter, the results of standard high-performance computing (HPC) benchmarks are presented in order to assess the performance characteristics of the various hardware and software components of an own built commodity-class Linux cluster. Introdu...

Full description

Bibliographic Details
Main Author: Nasr, Y. M. O.
Format: Thesis
Published: 2011
Subjects:
Online Access:http://pendeta.um.edu.my/client/default/search/results?qu=Computational+analysis+of+the+enantioselectivity+of+diels-alder+reactions&te=
http://studentsrepo.um.edu.my/3473/1/1._Title_page%2C_abstract%2C_content.pdf
http://studentsrepo.um.edu.my/3473/2/2._Chapter_1_%E2%80%93_6.pdf
_version_ 1848772423037485056
author Nasr, Y. M. O.
author_facet Nasr, Y. M. O.
author_sort Nasr, Y. M. O.
building UM Research Repository
collection Online Access
description This thesis is divided into six chapters. In the first chapter, the results of standard high-performance computing (HPC) benchmarks are presented in order to assess the performance characteristics of the various hardware and software components of an own built commodity-class Linux cluster. Introductions to enantioselective synthesis and quantum mechanical methods are provided in the second chapter. The third chapter gives insights into the enantioselectivity and mechanism of the organocatalytic Diels-Alder reaction using density functional theory (DFT) at the B3LYP/6-31G(d) level of theory. The fourth chapter attempts to rationalize the enantioselectivity and mechanism of the organocatalytic Diels-Alder reaction using various aspects of DFT. The organocatalytic solid-phase Diels-Alder reaction in terms of enantioselectivity and mechanism is theoretically investigated in the fifth chapter using the hybrid method ONIOM(QM:MM). The sixth chapter deals with the same organocatalyst but as applied to cyanosilylation of aldehydes. The mechanism and enantioselectivity of this reaction are also investigated by means of DFT at the B3LYP/6-31G(d) level of theory.
first_indexed 2025-11-14T13:26:16Z
format Thesis
id um-3473
institution University Malaya
institution_category Local University
last_indexed 2025-11-14T13:26:16Z
publishDate 2011
recordtype eprints
repository_type Digital Repository
spelling um-34732014-10-13T02:27:32Z Computational analysis of the enantioselectivity of diels-alder reactions involving chiral cationic oxazaborolidinium catalyst / Nasr Y.M. Omar Nasr, Y. M. O. Q Science (General) QD Chemistry This thesis is divided into six chapters. In the first chapter, the results of standard high-performance computing (HPC) benchmarks are presented in order to assess the performance characteristics of the various hardware and software components of an own built commodity-class Linux cluster. Introductions to enantioselective synthesis and quantum mechanical methods are provided in the second chapter. The third chapter gives insights into the enantioselectivity and mechanism of the organocatalytic Diels-Alder reaction using density functional theory (DFT) at the B3LYP/6-31G(d) level of theory. The fourth chapter attempts to rationalize the enantioselectivity and mechanism of the organocatalytic Diels-Alder reaction using various aspects of DFT. The organocatalytic solid-phase Diels-Alder reaction in terms of enantioselectivity and mechanism is theoretically investigated in the fifth chapter using the hybrid method ONIOM(QM:MM). The sixth chapter deals with the same organocatalyst but as applied to cyanosilylation of aldehydes. The mechanism and enantioselectivity of this reaction are also investigated by means of DFT at the B3LYP/6-31G(d) level of theory. 2011 Thesis NonPeerReviewed application/pdf http://studentsrepo.um.edu.my/3473/1/1._Title_page%2C_abstract%2C_content.pdf application/pdf http://studentsrepo.um.edu.my/3473/2/2._Chapter_1_%E2%80%93_6.pdf http://pendeta.um.edu.my/client/default/search/results?qu=Computational+analysis+of+the+enantioselectivity+of+diels-alder+reactions&te= Nasr, Y. M. O. (2011) Computational analysis of the enantioselectivity of diels-alder reactions involving chiral cationic oxazaborolidinium catalyst / Nasr Y.M. Omar. PhD thesis, University of Malaya. http://studentsrepo.um.edu.my/3473/
spellingShingle Q Science (General)
QD Chemistry
Nasr, Y. M. O.
Computational analysis of the enantioselectivity of diels-alder reactions involving chiral cationic oxazaborolidinium catalyst / Nasr Y.M. Omar
title Computational analysis of the enantioselectivity of diels-alder reactions involving chiral cationic oxazaborolidinium catalyst / Nasr Y.M. Omar
title_full Computational analysis of the enantioselectivity of diels-alder reactions involving chiral cationic oxazaborolidinium catalyst / Nasr Y.M. Omar
title_fullStr Computational analysis of the enantioselectivity of diels-alder reactions involving chiral cationic oxazaborolidinium catalyst / Nasr Y.M. Omar
title_full_unstemmed Computational analysis of the enantioselectivity of diels-alder reactions involving chiral cationic oxazaborolidinium catalyst / Nasr Y.M. Omar
title_short Computational analysis of the enantioselectivity of diels-alder reactions involving chiral cationic oxazaborolidinium catalyst / Nasr Y.M. Omar
title_sort computational analysis of the enantioselectivity of diels-alder reactions involving chiral cationic oxazaborolidinium catalyst / nasr y.m. omar
topic Q Science (General)
QD Chemistry
url http://pendeta.um.edu.my/client/default/search/results?qu=Computational+analysis+of+the+enantioselectivity+of+diels-alder+reactions&te=
http://pendeta.um.edu.my/client/default/search/results?qu=Computational+analysis+of+the+enantioselectivity+of+diels-alder+reactions&te=
http://studentsrepo.um.edu.my/3473/1/1._Title_page%2C_abstract%2C_content.pdf
http://studentsrepo.um.edu.my/3473/2/2._Chapter_1_%E2%80%93_6.pdf