Oluwole Familoni

Prof. Oluwole Familoni

orcid

Research Focus & Metrics

Academic Career Length

57Years (1970-Present)

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

Representative Publications

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15 April 2014 in Antioxidants
Verified
Journal Article
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SOSunday Okoh
Sunday Okoh
OAOlayinka Asekun
Olayinka Asekun
OFOluwole Familoni
Oluwole Familoni
AAAnthony Afolayan
Anthony Afolayan
Essential oils from plants have been proven safe as natural antioxidants, and few are already marketed as digestive enhancers as well as in prevention of several degenerative diseases. This study evaluated the antioxidant capacity of seed and shell essential oils of Abrus precatorius (L), a herb used for ethno-medicinal practices in Nigeria. The essential oils were obtained by hydro-distillation. The ability of the oils to act as hydrogen/electrons donor or scavenger of radicals were determined by in-vitro antioxidant assays using 2,2-diphenyl-2-picryl-hydrazyl free radical (DPPH.) scavenging; 2,2′-azino-bis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) radical scavenging; lipid peroxide and nitric oxide radicals scavenging assays. The IC50 of the seed and shell oils (2.10 mg/mL and 1.20 mg/mL respectively) showed that antioxidant activity is higher than that for the standard drugs (3.20 mg/mL and 3.40 mg/mL) for the nitric oxide scavenging assay. The lipid peroxidation radical activity of the oils were similar to vitamin C, weak DPPH and ABTS radical scavenging activities were discovered in comparison to vitamin C and rutin. Generally, in the four antioxidant assays, a significant correlation existed between concentrations of the oils and percentage inhibition of free radicals and lipid peroxidation. The composition of A. precatorius essential oils reported earlier may account for their antioxidant capacity.

1 January 1998 in Chemical Communications
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Journal Article
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OFOluwole Familoni
Oluwole Familoni
PKPerry T. Kaye
Perry T. Kaye
PKPhindile J. Klaas
Phindile J. Klaas
Reaction of 2-nitrobenzaldehyde with vinyl carbonyl compounds in the presence of 1,4-diazabicyclo[2.2.2]octane affords Baylis–Hillman products, catalytic reduction of which results in direct cyclisation to quinoline derivatives.

10 May 2001 in The Journal of Organic Chemistry
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Journal Article
Closed access
SMStephen L. MacNeil
Stephen L. MacNeil
OFOluwole Familoni
Oluwole Familoni
VSVictor Snieckus
Victor Snieckus

25 August 2018 in Medicinal Chemistry Research
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Journal Article
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MAMichael Afolayan
Michael Afolayan
RSRadhakrishnan Srivedavyasasri
Radhakrishnan Srivedavyasasri
OAOlayinka Asekun
Olayinka Asekun
OFOluwole Familoni
Oluwole Familoni
AOAbayomi Orishadipe
Abayomi Orishadipe
SRSamir Anis Ross
Samir Anis Ross

1 September 1997 in Synlett
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Journal Article
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OFOluwole Familoni
Oluwole Familoni
IIIleana Ionica
Ileana Ionica
JBJustin F. Bower
Justin F. Bower
VSVictor Snieckus
Victor Snieckus
An LDA-induced regiospecific and general conversion of diaryl ether 2-carboxamides 4 into substituted xanthones 5, including natural products, 2-hydroxy-1-methoxyxanthone (8) and 6-deoxy-jacareubin (14), is described.

1 January 1994 in Synlett
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Journal Article
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CQC. A. Quesnelle
C. A. Quesnelle
OFOluwole Familoni
Oluwole Familoni
VSV. Snieckus
V. Snieckus
Aryl zinc reagents, derived by directed ortho metalation, undergo cross coupling with aryl triflates under Ni(0) catalysis to provide a general, regiospecific method for the synthesis of diverse functionalized biaryls (Table).