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Synthesis of new B-lactams : a thesis

The syntheses of nocardicin analogues 31, 52 and cephalosporin analogue 95 are described. None of the above compounds showed the significant antibacterial activity. / The reaction of azidoacetyl chloride with various Schiff bases derived from phenylpropargyl aldehyde and substituted anilines, afforded (beta)-lactams in fair to good yields. / A new bicyclic (beta)-lactam 162 was synthesized. The key step involved the phosphorylation of the nitrogen on an N-unsubstituted (beta)-lactam ring. / A key intermediate 188 for the synthesis of monobactam analogue has been prepared.

Identiferoai:union.ndltd.org:LACETR/oai:collectionscanada.gc.ca:QMM.68713
Date January 1981
CreatorsLiu, Whi-Yu.
PublisherMcGill University
Source SetsLibrary and Archives Canada ETDs Repository / Centre d'archives des thèses électroniques de Bibliothèque et Archives Canada
LanguageEnglish
Detected LanguageEnglish
TypeElectronic Thesis or Dissertation
Formatapplication/pdf
CoverageDoctor of Philosophy (Department of Chemistry)
RightsAll items in eScholarship@McGill are protected by copyright with all rights reserved unless otherwise indicated.
Relationalephsysno: 000139378, proquestno: AAINL10269, Theses scanned by UMI/ProQuest.

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