Diastereoselective intramolecular aldol ring closures of threonine derivatives leading to densely functionalised pyroglutamates related to oxazolomycin
Intramolecular aldol reactions on oxazolidine templates derived from threonine may be used to generate libraries of densely functionalised pyroglutamates with a high level of diastereoselectivity; the oxazolidine precursors themselves are suitable for further direct manipulation by side chain alkyla...
Main Authors: | , , |
---|---|
Format: | Journal article |
Published: |
Royal Society of Chemistry
2014
|
_version_ | 1797055654834208768 |
---|---|
author | Heaviside, E Moloney, M Thompson, A |
author_facet | Heaviside, E Moloney, M Thompson, A |
author_sort | Heaviside, E |
collection | OXFORD |
description | Intramolecular aldol reactions on oxazolidine templates derived from threonine may be used to generate libraries of densely functionalised pyroglutamates with a high level of diastereoselectivity; the oxazolidine precursors themselves are suitable for further direct manipulation by side chain alkylation, permitting rapid access to cyclised products with several points of chemical diversity. Although these systems may be considered to be structural mimics of the functionalised pyroglutamate portion of oxazolomycin, little antibacterial activity against S. aureus and E. coli was found. These systems may additionally have application as three-dimensional fragments for drug discovery and development. |
first_indexed | 2024-03-06T19:12:52Z |
format | Journal article |
id | oxford-uuid:1758e3c8-fb58-4ddd-8c7c-87b82058be70 |
institution | University of Oxford |
last_indexed | 2024-03-06T19:12:52Z |
publishDate | 2014 |
publisher | Royal Society of Chemistry |
record_format | dspace |
spelling | oxford-uuid:1758e3c8-fb58-4ddd-8c7c-87b82058be702022-03-26T10:36:45ZDiastereoselective intramolecular aldol ring closures of threonine derivatives leading to densely functionalised pyroglutamates related to oxazolomycinJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:1758e3c8-fb58-4ddd-8c7c-87b82058be70Symplectic Elements at OxfordRoyal Society of Chemistry2014Heaviside, EMoloney, MThompson, AIntramolecular aldol reactions on oxazolidine templates derived from threonine may be used to generate libraries of densely functionalised pyroglutamates with a high level of diastereoselectivity; the oxazolidine precursors themselves are suitable for further direct manipulation by side chain alkylation, permitting rapid access to cyclised products with several points of chemical diversity. Although these systems may be considered to be structural mimics of the functionalised pyroglutamate portion of oxazolomycin, little antibacterial activity against S. aureus and E. coli was found. These systems may additionally have application as three-dimensional fragments for drug discovery and development. |
spellingShingle | Heaviside, E Moloney, M Thompson, A Diastereoselective intramolecular aldol ring closures of threonine derivatives leading to densely functionalised pyroglutamates related to oxazolomycin |
title | Diastereoselective intramolecular aldol ring closures of threonine derivatives leading to densely functionalised pyroglutamates related to oxazolomycin |
title_full | Diastereoselective intramolecular aldol ring closures of threonine derivatives leading to densely functionalised pyroglutamates related to oxazolomycin |
title_fullStr | Diastereoselective intramolecular aldol ring closures of threonine derivatives leading to densely functionalised pyroglutamates related to oxazolomycin |
title_full_unstemmed | Diastereoselective intramolecular aldol ring closures of threonine derivatives leading to densely functionalised pyroglutamates related to oxazolomycin |
title_short | Diastereoselective intramolecular aldol ring closures of threonine derivatives leading to densely functionalised pyroglutamates related to oxazolomycin |
title_sort | diastereoselective intramolecular aldol ring closures of threonine derivatives leading to densely functionalised pyroglutamates related to oxazolomycin |
work_keys_str_mv | AT heavisidee diastereoselectiveintramolecularaldolringclosuresofthreoninederivativesleadingtodenselyfunctionalisedpyroglutamatesrelatedtooxazolomycin AT moloneym diastereoselectiveintramolecularaldolringclosuresofthreoninederivativesleadingtodenselyfunctionalisedpyroglutamatesrelatedtooxazolomycin AT thompsona diastereoselectiveintramolecularaldolringclosuresofthreoninederivativesleadingtodenselyfunctionalisedpyroglutamatesrelatedtooxazolomycin |