Takamitsu Hosoya
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Explore the profile of Takamitsu Hosoya including associated specialties, affiliations and a list of published articles.
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162
Citations
1555
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Recent Articles
1.
Watanabe K, Uetake Y, Hata M, Kuwano A, Yamamoto R, Yamamoto Y, et al.
Small
. 2024 Dec;
:e2408747.
PMID: 39648606
For the development of highly multifunctionalized nanomaterials, the introduction of functional molecules on gold nanoclusters containing thiols preinstalled with connecting groupsconstitutes a promising approach. However, the uniform introduction of multiple...
2.
Taguchi J, Tokunaga K, Tabuchi H, Nishiyama T, Kii I, Hosoya T
Chem Commun (Camb)
. 2024 Nov;
60(98):14581-14584.
PMID: 39499544
A compact trialkyne platform with a silyl-protected 1,3-butadiynyl sulfide moiety and a terminal alkyne group has been developed for sequential regioselective transition metal-catalyzed triazole formation reactions with three azides. This...
3.
Shiino H, Tashiro S, Hashimoto M, Sakata Y, Hosoya T, Endo T, et al.
iScience
. 2024 Feb;
27(3):109189.
PMID: 38420588
Phospholipids are major components of biological membranes and play structural and regulatory roles in various biological processes. To determine the biological significance of phospholipids, the use of chemical inhibitors of...
4.
Watanabe K, Mao Q, Zhang Z, Hata M, Kodera M, Kitagishi H, et al.
Chem Sci
. 2024 Jan;
15(4):1402-1408.
PMID: 38274077
In this study, we successfully synthesized a small-sized gold nanocluster (2 nm) coated with homogeneous tripeptides bearing azido and amino groups that enable facile multifunctionalizations. Using sodium phenoxide to reduce...
5.
Niwa T, Takimoto T, Sakata Y, Hosoya T
Org Lett
. 2023 Nov;
25(45):8173-8177.
PMID: 37938808
Palladium-catalyzed -borylation of aryl halides, well-known as Miyaura borylation, is one of the reliable synthetic methods for organoborons. This reaction involves base-mediated nucleophilic activation of diboron that enables transmetalation of...
6.
Taguchi J, Okuyama T, Tomita S, Niwa T, Hosoya T
Org Lett
. 2023 Sep;
25(38):7030-7034.
PMID: 37712445
An efficient method for generating 3-triazenylarynes from -iodoaryl triflate-type precursors was developed. The generated arynes reacted with various arynophiles with high regioselectivity because of the triazenyl group. The 3-triazenylaryne precursors...
7.
Zhang Z, Niwa T, Watanabe K, Hosoya T
Angew Chem Int Ed Engl
. 2023 Apr;
62(22):e202302956.
PMID: 37097743
Aryl fluorides are expected to be useful as radiolabeling precursors due to their chemical stability and ready availability. However, direct radiolabeling via carbon-fluorine (C-F) bond cleavage is a challenging issue...
8.
Dubol M, Immenschuh J, Jonasson M, Takahashi K, Niwa T, Hosoya T, et al.
Compr Psychiatry
. 2023 Mar;
123:152381.
PMID: 36905856
Background: Of interest to women's mental health, a wealth of studies suggests sex differences in nicotine addiction and treatment response, but their psychoneuroendocrine underpinnings remain largely unknown. A pathway involving...
9.
Watanabe K, Kuratsu A, Hashizume D, Niwa T, Hosoya T
Commun Chem
. 2023 Jan;
5(1):91.
PMID: 36697938
The development of a conjugation method initiated by irradiation of long-wavelength light (>500 nm) to prepare densely functionalized molecules while avoiding undesired photodegradation has attracted considerable attention. Here we show...
10.
Kobayashi A, Matsuzawa T, Hosoya T, Yoshida S
RSC Adv
. 2023 Jan;
13(2):839-843.
PMID: 36686947
The interrupted Pummerer reaction of alkynyl sulfoxides with phenols is disclosed. A wide range of benzo[]furans were efficiently synthesized through unexplored electrophilic activation of the electron-deficient alkynyl sulfinyl group. Based...