Miku Oi
Overview
Explore the profile of Miku Oi including associated specialties, affiliations and a list of published articles.
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Articles
7
Citations
32
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0
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Recent Articles
1.
Jiang Y, El Khoury E, Pezacki A, Qian N, Oi M, Torrente L, et al.
J Am Chem Soc
. 2024 Nov;
146(49):33324-33337.
PMID: 39586074
Molecular imaging with analyte-responsive probes offers a powerful chemical approach to studying biological processes. Many reagents for bioimaging employ a fluorescence readout, but the relatively broad emission bands of this...
2.
Bonet-Aleta J, Encinas-Gimenez M, Oi M, Pezacki A, Sebastian V, de Martino A, et al.
ACS Appl Mater Interfaces
. 2024 Jun;
16(23):29844-29855.
PMID: 38829261
Copper plays critical roles as a metal active site cofactor and metalloallosteric signal for enzymes involved in cell proliferation and metabolism, making it an attractive target for cancer therapy. In...
3.
Kajino H, Nagatani T, Oi M, Kujirai T, Kurumizaka H, Nishiyama A, et al.
RSC Chem Biol
. 2021 Aug;
1(2):56-59.
PMID: 34458748
We report combinations of a DMAP-based catalyst and phenyl acetate with optimal electron density as a new chemical system for high-yield, selective synthetic acetylation of histone lysine residues. The utility...
4.
Nagashima N, Ozawa S, Furuta M, Oi M, Hori Y, Tomita T, et al.
Sci Adv
. 2021 Mar;
7(13).
PMID: 33762329
Protein degradation induced by small molecules by recruiting endogenous protein degradation systems, such as ubiquitin-proteasome systems, to disease-related proteins is an emerging concept to inhibit the function of undruggable proteins....
5.
Organocopper cross-coupling reaction for C-C bond formation on highly sterically hindered structures
Oi M, Takita R, Kanazawa J, Muranaka A, Wang C, Uchiyama M
Chem Sci
. 2019 Jul;
10(24):6107-6112.
PMID: 31360416
We describe a powerful, broadly applicable cross-coupling protocol that enables carbon-carbon bond formation at highly sterically hindered carbon centers (both sp and sp) by employing organocopper reagents under palladium catalysis....
6.
Tejo C, Pang J, Ong D, Oi M, Uchiyama M, Takita R, et al.
Chem Commun (Camb)
. 2018 Feb;
54(14):1782-1785.
PMID: 29383363
A new protocol for the dearylation of arylphosphine oxides was developed using sodium hydride (NaH) in the presence of lithium iodide (LiI). The transient sodium phosphinite could be functionalized with...
7.
Kaga A, Hayashi H, Hakamata H, Oi M, Uchiyama M, Takita R, et al.
Angew Chem Int Ed Engl
. 2017 Jul;
56(39):11807-11811.
PMID: 28741890
A method for the nucleophilic amination of methoxy arenes was established by using sodium hydride (NaH) in the presence of lithium iodide (LiI). This method offers an efficient route to...