Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Atsuhiro Takano"'
Autor:
Takatsugu Murata, Hisazumi Tsutsui, Takumi Yoshida, Hirokazu Kubota, Shintaro Hiraishi, Hiyo Natsukawa, Yuki Suzuki, Daiki Hiraga, Takahiro Mori, Yutaro Maekawa, Satoru Tateyama, Kiyotaka Toyoyama, Keiichi Ito, Kyohei Suzuki, Keita Yonekura, Natsumi Shibata, Teruyuki Sato, Yasutaka Tasaki, Takehiko Inohana, Atsuhiro Takano, Naoki Egashira, Masaki Honda, Yuma Umezaki, Isamu Shiina
Publikováno v:
ACS Omega, Vol 8, Iss 33, Pp 30789-30789 (2023)
Externí odkaz:
https://doaj.org/article/a4ff92c99e87498c92ccaec2ecbb52e7
Autor:
Takatsugu Murata, Hisazumi Tsutsui, Takumi Yoshida, Hirokazu Kubota, Shintaro Hiraishi, Hiyo Natsukawa, Yuki Suzuki, Daiki Hiraga, Takahiro Mori, Yutaro Maekawa, Satoru Tateyama, Kiyotaka Toyoyama, Keiichi Ito, Kyohei Suzuki, Keita Yonekura, Natsumi Shibata, Teruyuki Sato, Yasutaka Tasaki, Takehiko Inohana, Atsuhiro Takano, Naoki Egashira, Masaki Honda, Yuma Umezaki, Isamu Shiina
The first total synthesis of (+)-tanzawaic acid B, a natural polyketide bearing a pentadienoic ester and octalin moiety, has been accomplished. The synthetic improvement from previous synthetic conditions facilitated our gram-scale synthesis of the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4249a5ab572487b512014065a57b3520
https://doi.org/10.26434/chemrxiv-2022-p8hxs-v3
https://doi.org/10.26434/chemrxiv-2022-p8hxs-v3
Autor:
Takatsugu Murata, Hisazumi Tsutsui, Takumi Yoshida, Hirokazu Kubota, Shintaro Hiraishi, Hiyo Natsukawa, Yuki Suzuki, Daiki Hiraga, Takahiro Mori, Yutaro Maekawa, Satoru Tateyama, Kiyotaka Toyoyama, Keiichi Ito, Kyohei Suzuki, Keita Yonekura, Natsumi Shibata, Teruyuki Sato, Yasutaka Tasaki, Takehiko Inohana, Atsuhiro Takano, Isamu Shiina
The first total synthesis of (+)-tanzawaic acid B, a natural polyketide bearing a pentadienoic ester and octalin moiety, has been accomplished. The synthetic improvement from previous synthetic conditions facilitated our gram-scale synthesis of the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2df36efb8f26087b46cc827d60be59bc
https://doi.org/10.26434/chemrxiv-2022-p8hxs
https://doi.org/10.26434/chemrxiv-2022-p8hxs
Autor:
Takayuki Ohyoshi, Atsuhiro Takano, Imari Kikuchi, Tomotaka Ogura, Mayu Namiki, Yuto Miyazaki, Takahiro Hirano, Shota Konishi, Yuta Ebihara, Koichi Takeno, Ichiro Hayakawa, Hideo Kigoshi
Publikováno v:
Organicbiomolecular chemistry. 20(14)
An aplyronine A-swinholide A hybrid, consisting of the macrolactone part of aplyronine A and the side chain part of swinholide A, was designed, synthesized, and biologically evaluated. This hybrid induced protein-protein interactions between two majo
Autor:
Yuto Miyazaki, Koichi Takeno, Mayu Namiki, Atsuhiro Takano, Tomotaka Ogura, Takayuki Ohyoshi, Hideo Kigoshi, Yuta Ebihara, Ichiro Hayakawa
Publikováno v:
Chemical Communications. 54:9537-9540
An aplyronine A-swinholide A hybrid, consisting of the macrolactone part of aplyronine A and the side chain part of swinholide A, was designed, synthesized, and evaluated for biological activities. The hybrid retained strong cytotoxicity and actin-de
Publikováno v:
Tetrahedron Letters. 60:591-593
Swinhoeisterol A is a novel steroid with unusual 6/6/5/7 tetracyclic skeleton. The model compound with BCD rings is constructed by Friedel–Crafts acylation and an oxidative dearomatization as key steps.
Autor:
Susumu Kobayashi, Hiroshi Okuyama, Shinya Suzuki, Isao Shimizu, Takahiro Suzuki, Atsuhiro Takano
Publikováno v:
ChemInform. 45
The synthesis of a novel hydrocarbon, dibarrelane, has been accomplished in 11 steps via an intramolecular REDDA reaction of a masked o-benzoquinone, followed by Clemmensen reduction and Barton decarboxylation. The twisted structure of the tetracycli
Autor:
Susumu Kobayashi, Isao Shimizu, Atsuhiro Takano, Shinya Suzuki, Takahiro Suzuki, Hiroshi Okuyama
Publikováno v:
The Journal of organic chemistry. 79(6)
The synthesis of a novel hydrocarbon, dibarrelane, has been accomplished in 11 steps via an intramolecular REDDA reaction of a masked o-benzoquinone, followed by Clemmensen reduction and Barton decarboxylation. The twisted structure of the tetracycli
Autor:
Takahiro Suzuki, Hiroshi Okuyama, Atsuhiro Takano, Shinya Suzuki, Isao Shimizu, Susumu Kobayashi
Publikováno v:
Journal of Organic Chemistry; 3/21/2014, Vol. 79 Issue 6, p2803-2808, 6p