Výsledky vyhledávání - "Yuki Yoshinaga"

Rh(2)(II)-Catalyzed Intermolecular N-Aryl Aziridination of Olefins using Nonactivated N-Atom Precursors

Autor: Tianning Deng, Tala Malo, Tom G. Driver, Yuki Yoshinaga, Wrickban Mazumdar, Pooja B. Patel, Dana Malo, Donald J. Wink

Publikováno v: J Am Chem Soc

The development of the first intermolecular Rh2(II)-catalyzed aziridination of olefins using anilines as nonactivated N atom precursors and an iodine(III) reagent as the stoichiometric oxidant is reported. This reaction requires the transfer of an N-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b37aec61fb1a1d11752a16aabd74bce9
https://europepmc.org/articles/PMC9004320/

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Reactive Task Allocation and Planning for Quadrupedal and Wheeled Robot Teaming

Autor: Ziyi Zhou, Dong Jae Lee, Yuki Yoshinaga, Stephen Balakirsky, Dejun Guo, Ye Zhao

This paper takes the first step towards a reactive, hierarchical multi-robot task allocation and planning framework given a global Linear Temporal Logic specification. The capabilities of both quadrupedal and wheeled robots are leveraged via a hetero

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c51d34d87c9b885812f6b8a910804991

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Akademický článek

Rh2(II)-Catalyzed Intermolecular N-Aryl Aziridination of Olefins Using Nonactivated N Atom Precursors.

Autor: Tianning Deng, Mazumdar, Wrickban, Yuki Yoshinaga, Patel, Pooja B., Malo, Dana, Malo, Tala, Wink, Donald J., Driver, Tom G.

Publikováno v: Journal of the American Chemical Society; 11/17/2021, Vol. 143 Issue 45, p19149-19159, 11p

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Pleospdione, A Tricyclic Natural Product with Dense Oxygenation at the A-Ring: Total Synthesis and Incongruity of the Originally Assigned Structure and its C3-Epimer

Autor: Yoshimitsu Hashimoto, Takenori Kusumi, Hiroshi Takikawa, Yuki Yoshinaga, Yui Ishikawa, Keisuke Suzuki

Publikováno v: Bulletin of the Chemical Society of Japan. 89:941-954

Previously we developed a promising synthetic approach to complex polycyclic natural products, including aromatic polyketides derived from the type-II polyketide biosynthesis. The approach consists of three key steps; (1) cycloaddition or cycloconden

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ee580b3b4fd18ed7321282faaee9db3d
https://doi.org/10.1246/bcsj.20160134

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Catalytic asymmetric synthesis of the common amino acid component in the biosynthesis of tetrahydroisoquinoline alkaloids

Autor: Ryo Tanifuji, Hiroki Oguri, Yuki Yoshinaga, Kento Koketsu, Atsushi Minami, Hideaki Oikawa

Publikováno v: Tetrahedron Letters. 57:623-626

Biosynthetic assembly lines of tetrahydroisoquinoline alkaloids employ the tyrosine derivative, ( S )-2-amino-3-(3-hydroxy-4-methoxy-5-methylphenyl)propanoic acid, as a common amino acid building block. A catalytic asymmetric synthetic route to the c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c6ec5c62b23ec87727e5fafd1a57b9ff
https://doi.org/10.1016/j.tetlet.2015.12.110

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A formal total synthesis of the telomerase inhibitor dictyodendrin B

Autor: Shotaro Hirao, Yuki Yoshinaga, Masatomo Iwao, Fumito Ishibashi

Publikováno v: Tetrahedron Letters. 51(3):533-536

A formal synthesis of the telomerase inhibitory marine pyrrolocarbazole alkaloid dictyodendrin B is described. The key features are consecutive palladium-catalyzed cross-coupling reactions and intramolecular reductive coupling reaction to construct t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42f62b87edd11bea5d1206fb574d6156
https://nagasaki-u.repo.nii.ac.jp/records/15231

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