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Synthesis, antimalarial evaluation and structure-activity relationship in a series of dibenzlmethylamine (Dibemethin) derivatives of 4-amino-7-chloroquinoline

Includes abstract.

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Bibliographic Details
Main Author: Zishiri, Vincent Kudakwashe
Other Authors: Egan, Timothy J
Format: Thesis
Language:English
Published: Department of Chemistry 2014
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access_status_str Open Access
author Zishiri, Vincent Kudakwashe
author2 Egan, Timothy J
author_browse Egan, Timothy J
Zishiri, Vincent Kudakwashe
author_facet Egan, Timothy J
Zishiri, Vincent Kudakwashe
author_sort Zishiri, Vincent Kudakwashe
collection Thesis
description Includes abstract.
format Thesis
id oai:open.uct.ac.za:11427/6280
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:33:59.204Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
publisher Department of Chemistry
publisherStr Department of Chemistry
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/6280 Synthesis, antimalarial evaluation and structure-activity relationship in a series of dibenzlmethylamine (Dibemethin) derivatives of 4-amino-7-chloroquinoline Zishiri, Vincent Kudakwashe Egan, Timothy J Hunter, Roger Chemistry Includes abstract. Includes bibliographical references (leaves 138-154). A series of twelve 4-amino-7-chloroquinolines containing (N, N-dibenzylmethylamine) dibemethin side chains attached to the amino group of the quinoline were synthesized by reaction of aminomethyl dibemethins with 4,7-dichloroquinoline to give “dibemethinoquines”. The attachment between the quinoline ring and the side chain was varied from ortho, to meta to para. The aminomethyl dibemethin side chains were synthesized using the Staudinger reduction of azides or the reductive amination via oxime of an aldehyde. Derivatives in which the para substituent on the terminal phenyl ring were altered from the parent compound (X = H) by replacement with Cl, OCH₃ orNMe₂ group were also synthesized. The choice of substituents was based on the Topliss scheme. 2014-08-13T14:25:24Z 2014-08-13T14:25:24Z 2008 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/6280 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
Zishiri, Vincent Kudakwashe
Synthesis, antimalarial evaluation and structure-activity relationship in a series of dibenzlmethylamine (Dibemethin) derivatives of 4-amino-7-chloroquinoline
thesis_degree_str Doctoral
title Synthesis, antimalarial evaluation and structure-activity relationship in a series of dibenzlmethylamine (Dibemethin) derivatives of 4-amino-7-chloroquinoline
title_full Synthesis, antimalarial evaluation and structure-activity relationship in a series of dibenzlmethylamine (Dibemethin) derivatives of 4-amino-7-chloroquinoline
title_fullStr Synthesis, antimalarial evaluation and structure-activity relationship in a series of dibenzlmethylamine (Dibemethin) derivatives of 4-amino-7-chloroquinoline
title_full_unstemmed Synthesis, antimalarial evaluation and structure-activity relationship in a series of dibenzlmethylamine (Dibemethin) derivatives of 4-amino-7-chloroquinoline
title_short Synthesis, antimalarial evaluation and structure-activity relationship in a series of dibenzlmethylamine (Dibemethin) derivatives of 4-amino-7-chloroquinoline
title_sort synthesis antimalarial evaluation and structure activity relationship in a series of dibenzlmethylamine dibemethin derivatives of 4 amino 7 chloroquinoline
topic Chemistry
url http://hdl.handle.net/11427/6280
work_keys_str_mv AT zishirivincentkudakwashe synthesisantimalarialevaluationandstructureactivityrelationshipinaseriesofdibenzlmethylaminedibemethinderivativesof4amino7chloroquinoline