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Yoshiki Morimoto

Showing results (1-10 of 48) with videos related to

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Organic & Biomolecular Chemistry|May 3, 2008
The role of chemical synthesis in structure elucidation of oxasqualenoidsYoshiki Morimoto
Angewandte Chemie (International Ed. in English)|February 28, 2009
Total synthesis and determination of the absolute configuration of (+)-omaezakianolYoshiki Morimoto, Tatsuya Okita, Hitomi Kambara
Chirality|July 12, 2002
Asymmetric total synthesis of highly symmetric squalene-derived cytotoxic polyethersYoshiki Morimoto, Takamasa Kinoshita, Toshiyuki Iwai
Journal of the American Chemical Society|April 21, 2005
Total synthesis and complete assignment of the stereostructure of a cytotoxic bromotriterpene polyether (+)-aurilolYoshiki Morimoto, Yoshihiro Nishikawa, Mamoru Takaishi
Organic Letters|July 19, 2003
Total synthesis and assignment of the double-bond position and absolute configuration of (-)-pyrinodemin AYoshiki Morimoto, Satoru Kitao, Tatsuya Okita, et al.
Msphere|August 27, 2024
A nitrogenase-like enzyme is involved in the novel anaerobic assimilation pathway of a sulfonate, isethionate, in the photosynthetic bacterium <i>Rhodobacter capsulatus</i>Yoshiki Morimoto, Kazuma Uesaka, Yuichi Fujita, et al.
Organic Letters|April 23, 2005
Structures, biological activities, and total syntheses of 13-hydroxy- and 13-acetoxy-14-nordehydrocacalohastine, novel modified furanoeremophilane-type sesquiterpenes from Trichilia cuneataMatsumi Doe, Taku Shibue, Hiroyuki Haraguchi, et al.
Chemistry, an Asian Journal|October 27, 2021
Asymmetric Total Syntheses, Stereostructures, and Cytotoxicities of Marine Bromotriterpenoids Aplysiol B (Laurenmariannol) and Saiyacenol AKento Nishikibe, Keisuke Nishikawa, Momochika Kumagai, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|June 2, 2021
Establishing a "Ring-Size-Divergent" Synthetic Strategy: Synthesis, Structural Revision, and Absolute Configuration of FeroniellinsKeisuke Nishikawa, Toshiki Niwa, Kento Nishikibe, et al.
RSC Advances|May 11, 2022
Formal total synthesis of histrionicotoxin alkaloids <i>via</i> Hg(OTf)<sub>2</sub>-catalyzed cycloisomerization and SmI<sub>2</sub>-induced ring expansionKunihiro Matsumura, Keisuke Nishikawa, Hiroaki Yoshida, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Organic & Biomolecular Chemistry|May 3, 2008
The role of chemical synthesis in structure elucidation of oxasqualenoidsYoshiki Morimoto
Angewandte Chemie (International Ed. in English)|February 28, 2009
Total synthesis and determination of the absolute configuration of (+)-omaezakianolYoshiki Morimoto, Tatsuya Okita, Hitomi Kambara
Chirality|July 12, 2002
Asymmetric total synthesis of highly symmetric squalene-derived cytotoxic polyethersYoshiki Morimoto, Takamasa Kinoshita, Toshiyuki Iwai
Journal of the American Chemical Society|April 21, 2005
Total synthesis and complete assignment of the stereostructure of a cytotoxic bromotriterpene polyether (+)-aurilolYoshiki Morimoto, Yoshihiro Nishikawa, Mamoru Takaishi
Organic Letters|July 19, 2003
Total synthesis and assignment of the double-bond position and absolute configuration of (-)-pyrinodemin AYoshiki Morimoto, Satoru Kitao, Tatsuya Okita, et al.
Msphere|August 27, 2024
A nitrogenase-like enzyme is involved in the novel anaerobic assimilation pathway of a sulfonate, isethionate, in the photosynthetic bacterium <i>Rhodobacter capsulatus</i>Yoshiki Morimoto, Kazuma Uesaka, Yuichi Fujita, et al.
Organic Letters|April 23, 2005
Structures, biological activities, and total syntheses of 13-hydroxy- and 13-acetoxy-14-nordehydrocacalohastine, novel modified furanoeremophilane-type sesquiterpenes from Trichilia cuneataMatsumi Doe, Taku Shibue, Hiroyuki Haraguchi, et al.
Chemistry, an Asian Journal|October 27, 2021
Asymmetric Total Syntheses, Stereostructures, and Cytotoxicities of Marine Bromotriterpenoids Aplysiol B (Laurenmariannol) and Saiyacenol AKento Nishikibe, Keisuke Nishikawa, Momochika Kumagai, et al.
Chemistry (Weinheim an Der Bergstrasse, Germany)|June 2, 2021
Establishing a "Ring-Size-Divergent" Synthetic Strategy: Synthesis, Structural Revision, and Absolute Configuration of FeroniellinsKeisuke Nishikawa, Toshiki Niwa, Kento Nishikibe, et al.
RSC Advances|May 11, 2022
Formal total synthesis of histrionicotoxin alkaloids <i>via</i> Hg(OTf)<sub>2</sub>-catalyzed cycloisomerization and SmI<sub>2</sub>-induced ring expansionKunihiro Matsumura, Keisuke Nishikawa, Hiroaki Yoshida, et al.
Pageof 5