Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Shade J. Olorunshola"'
Autor:
Olayinka O. Ajani, King T. Iyaye, Damilola V. Aderohunmu, Ifedolapo O. Olanrewaju, Markus W. Germann, Shade J. Olorunshola, Babatunde L. Bello
Publikováno v:
Arabian Journal of Chemistry, Vol 13, Iss 1, Pp 1809-1820 (2020)
Microwave-assisted approach was utilized as green approach to access a series of 2-propylquinoline-4-carbohydrazide hydrazone derivatives 10a-j of aromatic and heteroaromatic aldehydes in highly encouraging yields. It involved four steps reaction whi
Externí odkaz:
https://doaj.org/article/0c3c984f1af041b298c785e88dca2701
Autor:
Olayinka O. Ajani, Maria M. Akande, Natasha October, Tolutope O. Siyanbola, Damilola V. Aderohunmu, Anuoluwa A. Akinsiku, Shade J. Olorunshola
Publikováno v:
Arab Journal of Basic and Applied Sciences, Vol 26, Iss 1, Pp 362-375 (2019)
A variety of 3-(5-(substituted-phenyl)-4,5-dihydro-1H-pyrazol-3-yl)-2H-chromen-2-one derivatives 3a–j were synthesized through microwave assisted thermal annulation of corresponding α,β-unsaturated ketones (chalcones) 2a–j via hydrazinolysis. C
Externí odkaz:
https://doaj.org/article/6e46e7a929274c168ea071822a6b7688
Autor:
Olayinka O. Ajani, Olayinka O. Tolu-Bolaji, Shade J. Olorunshola, Yuxia Zhao, Damilola V. Aderohunmu
Publikováno v:
Journal of Advanced Research, Vol 8, Iss 6, Pp 703-712 (2017)
The aim of this present study was to synthesize 2-substituted and 1,2-disubstituted benzimidazole derivatives to investigate their antibacterial diversity for possible future drug design. The structure-based design of precursors 2-(1H-benzimidazol-2-
Externí odkaz:
https://doaj.org/article/b656d8c9634640d98f267a62c6ad9fa8
Autor:
Babatunde L. Bello, Shade J. Olorunshola, Damilola V. Aderohunmu, Olayinka O. Ajani, I. O. Olanrewaju, Markus W. Germann, King T. Iyaye
Publikováno v:
Arabian Journal of Chemistry, Vol 13, Iss 1, Pp 1809-1820 (2020)
Microwave-assisted approach was utilized as green approach to access a series of 2-propylquinoline-4-carbohydrazide hydrazone derivatives 10a-j of aromatic and heteroaromatic aldehydes in highly encouraging yields. It involved four steps reaction whi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9634017e915f2278409dcc154f72ac80
https://doi.org/10.1016/j.arabjc.2018.01.015
https://doi.org/10.1016/j.arabjc.2018.01.015
Autor:
Moses Emetere, Samuel Eshorame Sanni, Shade J. Olorunshola, Ayomipo P. Ewetade, Emeka Emmanuel Okoro, Taiwo S. Olugbenga, Oluranti Agboola
Publikováno v:
Materials Today Communications. 19:238-251
Microbialcorrosionoftheexternalsurfaceofcarbonsteelpipeswasinvestigatedusingsodiumtungstate,sodium nitrite and zinc nitrite as individual and combined inhibitors. The study involved carbon steel pipes in contact with Acidithiobaccillus thiooxidan. In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7af4fc6617058f83a32d6696324c33a1
https://doi.org/10.1016/j.mtcomm.2018.12.010
https://doi.org/10.1016/j.mtcomm.2018.12.010
Autor:
Shade J. Olorunshola, T. O. Siyanbola, Natasha October, A.A. Akinsiku, Maria M. Akande, Olayinka O. Ajani, Damilola V. Aderohunmu
Publikováno v:
Arab Journal of Basic and Applied Sciences, Vol 26, Iss 1, Pp 362-375 (2019)
A variety of 3-(5-(substituted-phenyl)-4,5-dihydro-1H-pyrazol-3-yl)-2H-chromen-2-one derivatives 3a–j were synthesized through microwave assisted thermal annulation of corresponding α,β-unsaturated ketones (chalcones) 2a–j via hydrazinolysis. C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::078d5d7b94ffb300656d8b49c089f8e0
https://doi.org/10.1080/25765299.2019.1632141
https://doi.org/10.1080/25765299.2019.1632141
Autor:
Kolawole Oluseyi Ajanaku, F.E. Owolabi, Shade J. Olorunshola, Benedict I. Ita, A. Edobor-Osoh, P. de la Presa
Publikováno v:
MethodsX, Vol 6, Iss, Pp 682-689 (2019)
We report the structural, morphological and optical activities of a paramagnetic manganite (La0.33Ca0.67MnO3) synthesized at 900 °C. A simple method of formation of complex was employed. A complex was formed between a pre-prepared manganite dissolve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5f82f28faf832f990cf04eef3060de0
https://doi.org/10.1016/j.mex.2019.03.004
https://doi.org/10.1016/j.mex.2019.03.004
Autor:
Oluwatosin Yemisi Audu, Alice O. Kuye, King T. Iyaye, Shade J. Olorunshola, Olayinka O. Ajani, I. O. Olanrewaju
Publikováno v:
Journal of Heterocyclic Chemistry. 55:302-312
The World Academy of Sciences (TWAS) was gratefully acknowledged by OOA for the sponsorship of this present work under the TWAS Research Grant for Individual Scientists in Basic Sciences Programme (grant no.: 14-069 RG/CHE/AF/AC_1).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::51f5895082698cbd4c59f2c32c82db8e
https://doi.org/10.1002/jhet.3050
https://doi.org/10.1002/jhet.3050
Autor:
Shade J. Olorunshola, Damilola V. Aderohunmu, Olayinka O. Tolu-Bolaji, Olayinka O. Ajani, Yuxia Zhao
Publikováno v:
Journal of Advanced Research, Vol 8, Iss 6, Pp 703-712 (2017)
The aim of this present study was to synthesize 2-substituted and 1,2-disubstituted benzimidazole derivatives to investigate their antibacterial diversity for possible future drug design. The structure-based design of precursors 2-(1H-benzimidazol-2-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9608e4f56a697883271f5b93963668f7
http://www.sciencedirect.com/science/article/pii/S2090123217301030
http://www.sciencedirect.com/science/article/pii/S2090123217301030
Autor:
Dominic E. Azuh, Shade J. Olorunshola, J.A.O Olugbuyiro, Raphael C. Mordi, Samuel L. Oputah, Kolawole Oluseyi Ajanaku
Publikováno v:
Oriental Journal of Physical Sciences. 1:05-09
Phytochemical and antibacterial properties of ethanolic extract of the seeds of African Star Apple (Chrysophyllum albidum) were investigated. The phytochemical result revealed the presence of saponins, carbohydrates, flavonoids, quinones, cardiac gly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::768071a52533ddd8d5f0a3aaccb130f9
https://doi.org/10.13005/ojps01.0102.02
https://doi.org/10.13005/ojps01.0102.02