Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/22986
Title: Synthesis of N-Propargyl Iminosugar Scaffolds for Compound Library Generation using Click Chemistry
Contributor(s): Wilkinson, Brendan  (author)orcid ; Bornaghi, Laurent F (author); Lopez, Marie (author); Healy, Peter C (author); Poulsen, Sally-Ann (author); Houston, Todd A (author)
Publication Date: 2010
DOI: 10.1071/ch09426
Handle Link: https://hdl.handle.net/1959.11/22986
Abstract: We have developed an efficient synthesis of N-propargyl iminosugars for use in diversity-oriented library development. Through a common, crystalline intermediate both piperidine and azepane scaffolds can be prepared with an alkyne functional group, allowing for further elaboration through reaction with azides.
Publication Type: Journal Article
Source of Publication: Australian Journal of Chemistry, 63(5), p. 821-829
Publisher: CSIRO Publishing
Place of Publication: Australia
ISSN: 1445-0038
0004-9425
Fields of Research (FoR) 2008: 030503 Organic Chemical Synthesis
030401 Biologically Active Molecules
030499 Medicinal and Biomolecular Chemistry not elsewhere classified
Fields of Research (FoR) 2020: 340401 Biologically active molecules
340503 Organic chemical synthesis
340499 Medicinal and biomolecular chemistry not elsewhere classified
Socio-Economic Objective (SEO) 2008: 970106 Expanding Knowledge in the Biological Sciences
970103 Expanding Knowledge in the Chemical Sciences
929999 Health not elsewhere classified
Socio-Economic Objective (SEO) 2020: 280102 Expanding knowledge in the biological sciences
200199 Clinical health not elsewhere classified
280105 Expanding knowledge in the chemical sciences
Peer Reviewed: Yes
HERDC Category Description: C1 Refereed Article in a Scholarly Journal
Appears in Collections:Journal Article
School of Science and Technology

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