David Gammon

Prof. David Gammon


Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 March 2010 in Green Chemistry
Verified
Journal Article
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PLPieter Levecque
Pieter Levecque
DGDavid Gammon
David Gammon
PJPierre Jacobs
Pierre Jacobs
DVDirk De Vos
Dirk De Vos
BSBert Sels
Bert Sels
The Ferrier rearrangement of a selection of protected glycals was successfully performed using a commercially available H-USY zeolite CBV-720 as catalyst, selected after screening a range of similar catalysts. By incorporating either alcohols, thiophenol, trimethylsilyl azide or allyltrimethylsilane in the reaction it was shown that a range of O-, S-, N- and C-glycosides could be formed. With benzylated glucal and galactal in particular, use of the CBV-720 catalyst led to significantly higher yields of the 2,3-dehydroglycosides than previously reported.

1 April 2010 in Bioorganic & Medicinal Chemistry
Verified
Journal Article
Closed access
DGDavid Gammon
David Gammon
DSDaniel J. Steenkamp
Daniel J. Steenkamp
Vuyo MavumengwanaVuyo Mavumengwana
Vuyo Mavumengwana
MMMohlopheni J. Marakalala
Mohlopheni J. Marakalala
TMTheophilus T. Mudzunga
Theophilus T. Mudzunga
MMMuganza Munyololo
Muganza Munyololo

31 May 2007 in Journal of Carbohydrate Chemistry
Verified
Journal Article
Closed access
DGDavid Gammon
David Gammon
HKHenok H. Kinfe
Henok H. Kinfe
DVDirk E. De Vos
Dirk E. De Vos
PJPierre A. Jacobs
Pierre A. Jacobs
BSBert F. Sels
Bert F. Sels
Protected glycals and α‐1,2‐cyclopropanated sugars were converted in high yields and selectivities in less than 2 h at low temperatures to 2‐deoxy‐2‐iodoglycosyl acetates or novel 2‐deoxy‐2‐iodomethylglycosyl acetates using the simple, inexpensive reagent mixture of ammonium iodide, hydrogen peroxide, and acetic anhydride/acetic acid in acetonitrile. The protected glycals gave rise to 2‐deoxy‐2‐bromoglycosyl acetates when ammonium bromide was used instead of the iodide, although longer reaction times were required and selectivities were inferior. Other simple olefins such as styrene and indene were also converted to their corresponding 1,2‐trans‐iodoacetates.

7 December 2010 in Advanced Synthesis & Catalysis
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Journal Article
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ADAnneleen L. W. Demuynck
Anneleen L. W. Demuynck
PLPieter Levecque
Pieter Levecque
AKAklilu Kidane
Aklilu Kidane
DGDavid Gammon
David Gammon
ESEugene Sickle
Eugene Sickle
BSBert F. Sels
Bert F. Sels

7 July 2008 in Advanced Synthesis & Catalysis
Verified
Journal Article
Closed access
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PLPieter Levecque
Pieter Levecque
DGDavid Gammon
David Gammon
HKHenok Hadgu Kinfe
Henok Hadgu Kinfe
PJPierre Jacobs
Pierre Jacobs
DVDirk De Vos
Dirk De Vos
BSBert Sels
Bert Sels

29 June 2020 in Molecules
Verified
Journal Article
Open access
PDF file
KAKojo Acquah
Kojo Acquah
DBDenzil R. Beukes
Denzil R. Beukes
DWDigby Warner
Digby Warner
PMPaul R. Meyers
Paul R. Meyers
SSSuthananda Sunassee
Suthananda Sunassee
DGDavid Gammon
David Gammon
In this paper, we report on the chemistry of the rare South African Actinomycete Kribbella speibonae strain SK5, a prolific producer of hydroxamate siderophores and their congeners. Two new analogues, dehydroxylated desferrioxamines, speibonoxamine 1 and desoxy-desferrioxamine D1 2, have been isolated, together with four known hydroxamates, desferrioxamine D1 3, desferrioxamine B 4, desoxy-nocardamine 5 and nocardamine 6, and a diketopiperazine (DKP) 7. The structures of 1–7 were characterized by the analysis of HRESIMS and 1D and 2D NMR data, as well as by comparison with the relevant literature. Three new dehydroxy desferrioxamine derivatives 8–10 were tentatively identified in the molecular network of K. speibonae strain SK5 extracts, and structures were proposed based on their MS/MS fragmentation patterns. A plausible spb biosynthetic pathway was proposed. To the best of our knowledge, this is the first report of the isolation of desferrioxamines from the actinobacterial genus Kribbella.