Zobrazeno 1 - 10
of 39
pro vyhledávání: '"phosphine-borane complexes"'
Publikováno v:
Pharmaceuticals, Vol 17, Iss 11, p 1417 (2024)
Background: Neurodegenerative diseases can cause vision loss by damaging retinal ganglion cells in the optic nerve. Novel phosphine-borane compounds (PBs) can protect these cells from oxidative stress via the reduction of disulfide bonds. However, th
Externí odkaz:
https://doaj.org/article/8fa3fe4636d54c968a203051db3e5b84
Akademický článek
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Publikováno v:
Inorganics, Vol 11, Iss 7, p 310 (2023)
Understanding the complex mechanisms underlying redox-mediated biological processes is a fundamental pillar of cellular biology. We describe the identification and quantification of disulfide formation and reduction in response to phosphine–borane
Externí odkaz:
https://doaj.org/article/057102299fde4c8d98c35690fb768ac5
Autor:
Kateryna D. Butova, Vladislav V. Bahonsky, Raisa I. Yurchenko, Maryna M. Moroz, Andrey A. Fokin
Publikováno v:
Журнал органічної та фармацевтичної хімії, Vol 18, Iss 3, Pp 35-38 (2020)
Despite diamondoid phosphines have found many synthetic applications and are even available commercially the chemistry of chiral diamondoid phosphines remains largely unexplored. Aim. To develop the convenient preparative method for the preparatio
Externí odkaz:
https://doaj.org/article/a727772952524552b17c10d11fa5979b
Akademický článek
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Autor:
Bahonsky, Vladislav V., Butov, Sergey O., Moroz, Maryna M., Fokin, Andrey A., Butova, Kateryna D., Yurchenko, Raisa I.
Publikováno v:
Журнал органічної та фармацевтичної хімії; Том 18, № 3(71) (2020); 35-38
Journal of Organic and Pharmaceutical Chemistry; Том 18, № 3(71) (2020); 35-38
Журнал органической и фармацевтической химии; Том 18, № 3(71) (2020); 35-38
Journal of Organic and Pharmaceutical Chemistry; Том 18, № 3(71) (2020); 35-38
Журнал органической и фармацевтической химии; Том 18, № 3(71) (2020); 35-38
Despite diamondoid phosphines have found many synthetic applications and are even available commercially the chemistry of chiral diamondoid phosphines remains largely unexplored.Aim. To develop the convenient preparative method for the preparation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=scientific_p::f15078f799d0b52b754acc5e4a0d9f05
http://ophcj.nuph.edu.ua/article/view/ophcj.20.199828
http://ophcj.nuph.edu.ua/article/view/ophcj.20.199828
Publikováno v:
Redox Biology
Exposure to radiation can damage endothelial cells in the irradiated area via the production of reactive oxygen species. We synthesized phosphine–borane complexes that reduce disulfide bonds and had previously been shown to interfere with redox-med
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::276f95c385cfebee3589949816f48b97
https://pubmed.ncbi.nlm.nih.gov/26188467
https://pubmed.ncbi.nlm.nih.gov/26188467
Publikováno v:
Journal of Organometallic Chemistry. 691(24-25)
Ruthenium-catalysed olefin cross-metathesis can be used to synthesise structurally diverse acyclic phosphines protected as their borane complexes. Homodimerisations have been investigated and proved successful only for the allyl-substituted borane-pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d096ee0621f1441e12de3d5973d2c2f8
http://ora.ox.ac.uk/objects/uuid:d398ecc5-0640-4f2c-8ba4-9eb3622aab3c
http://ora.ox.ac.uk/objects/uuid:d398ecc5-0640-4f2c-8ba4-9eb3622aab3c
Publikováno v:
Organic letters. 8(8)
[reaction: see text] A general new method for the one-pot preparation of secondary phosphines 11 and in situ generation of their borane complexes 12 is described. This method consists of the sequential addition, at room temperature, of equivalent amo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bdb8c0fe60d690537e8dd76651f861b
https://pubmed.ncbi.nlm.nih.gov/16597139
https://pubmed.ncbi.nlm.nih.gov/16597139