Výsledky vyhledávání - "Taro Matsuyama"

Akademický článek

DFT Study on Retigerane-Type Sesterterpenoid Biosynthesis: Initial Conformation of GFPP Regulates Biosynthetic Pathway, Ring-Construction Order and Stereochemistry

Autor: Yuichiro Watanabe, Takahiro Hashishin, Hajime Sato, Taro Matsuyama, Masaya Nakajima, Jun-ichi Haruta, Masanobu Uchiyama

Publikováno v: JACS Au, Vol 4, Iss 9, Pp 3484-3491 (2024)

Externí odkaz: https://doaj.org/article/b51a23b358284174b0b58a03eea8cbb4

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Revision of the Peniroquesine Biosynthetic Pathway by Retro-Biosynthetic Theoretical Analysis: Ring Strain Controls the Unique Carbocation Rearrangement Cascade

Autor: Taro Matsuyama, Ko Togashi, Moe Nakano, Hajime Sato, Masanobu Uchiyama

Publikováno v: JACS Au.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f91b593f8b556a8e15f68f10592da54b
https://doi.org/10.1021/jacsau.3c00039

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Elucidation of Late-Stage Biosynthesis of Phomoidride: Proposal of Cyclization Mechanism Affording Characteristic Nine-Membered Ring of Fungal Dimeric Anhydride

Autor: Shintaro Yamamoto, Taro Matsuyama, Taro Ozaki, Junya Takino, Hajime Sato, Masanobu Uchiyama, Atsushi Minami, Hideaki Oikawa

Publikováno v: Journal of the American Chemical Society. 144(46)

Antihypercholesterolemic agent phomoidride (PMD) B has a highly elaborated bicyclo[4.3.1]deca-1,6-diene core scaffold derived from dimeric anhydride with a nine-membered ring. This report elucidated the late stage transformation from an anhydride mon

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f9863f8866c4dfed552d81fc84cb6f2
https://pubmed.ncbi.nlm.nih.gov/36374185

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Molecular and Computational Bases for Spirofuranone Formation in Setosusin Biosynthesis

Autor: Masanobu Uchiyama, Hajime Sato, Taro Matsuyama, Yudai Matsuda, Kazunori Miyamoto, Dexiu Yan, Xingxing Wei, Pui Man Chan

Publikováno v: Journal of the American Chemical Society. 143(42)

The 3(2H)-furanone unit is observed in many biologically active natural products, as represented by the antifungal medication griseofulvin. Setosusin (1) is a fungal meroditerpenoid featuring a unique spiro-fused 3(2H)-furanone moiety; however, the b

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::028a97109416580c4b7e4b0c98ed1c82
https://pubmed.ncbi.nlm.nih.gov/34644070

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Akademický článek

Molecular and Computational Bases for Spirofuranone Formation in Setosusin Biosynthesis.

Autor: XingxingWei, Taro Matsuyama, Hajime Sato, Dexiu Yan, Pui Man Chan, Kazunori Miyamoto, Masanobu Uchiyama, Yudai Matsuda

Publikováno v: Journal of the American Chemical Society; 10/27/2021, Vol. 143 Issue 42, p17708-17715, 8p

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Electrochemical immobilization of Fluorescent labelled probe molecules on a FTO surface for affinity detection based on photo-excited current

Autor: Ryo Wakabayashi, Sho-taro Matsuyama, Tetsuya Haruyama, Takeshi Cho

Publikováno v: IOP Conference Series: Materials Science and Engineering. 18:212005

Photo-excited current can be generated at a molecular interface between a photo-excited molecules and a semi-conductive material in appropriate condition. The system has been recognized for promoting photo-energy devices such as an organic dye sensit

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::646043e6b99818c61c6c352dd3f3e323
https://doi.org/10.1088/1757-899x/18/21/212005

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