Stereochemical Determination of Acyclic Structures Based on Carbon-Proton Spin-Coupling Constants. A Method of Configuration Analysis for Natural Products.
- N. Matsumori, D. Kaneno, M. Murata, Hideshi Nakamura, K. Tachibana
- ChemistryJournal of Organic Chemistry
- 20 January 1999
This J-based configuration analysis was applied to the stereochemical elucidation of carboxylic acid 5 derived from zooxanthellatoxin and proven to be a practical method even for natural products with complicated structures.
Okadaic acid, a cytotoxic polyether from two marine sponges of the genus Halichondria
- K. Tachibana, P. Scheuer, F. Schmitz
- 1 May 1981
Pathological effects on mice by gambierol, possibly one of the ciguatera toxins.
- E. Ito, F. Suzuki-Toyota, M. Sasaki
- 1 December 2003
Cholesterol-independent membrane disruption caused by triterpenoid saponins.
- M. Hu, K. Konoki, K. Tachibana
- Chemistry, BiologyBiochimica et Biophysica Acta
- 19 January 1996
The Complete Structure of Maitotoxin, Part II: Configuration of the C135 ? C142 Side Chain and Absolute Configuration of the Entire Molecule
- Taro Nonomura, M. Sasaki, N. Matsumori, M. Murata, K. Tachibana, T. Yasumoto
- 1 August 1996
Isolation and chemical structure of amphidinol 2, a potent hemolytic compound from marine dinoflagellate Amphidinium klebsii
- G. K. Paul, N. Matsumori, M. Murata, K. Tachibana
- 28 August 1995
Shark repellent lipophilic constituents in the defense secretion of the Moses sole (Pardachirus marmoratus).
- K. Tachibana, S. Gruber
Chemical structures of amphidinols 5 and 6 isolated from marine dinoflagellate Amphidinium klebsii and their cholesterol-dependent membrane disruption
- K. Gopal, N. Matsumori, K. Konoki, M. Murata, K. Tachibana
- 1 December 1997
Cloning of modular type I polyketide synthase genes from salinomycin producing strain of Streptomyces albus.
- M. Izumikawa, M. Murata, K. Tachibana, Y. Ebizuka, I. Fujii
- Biology, ChemistryBioorganic & Medicinal Chemistry
- 5 August 2003
Ophiobolin O and 6-Epi-Ophiobolin O, Two New Cytotoxic Sesterterpenes from the Marine Derived Fungus Aspergillus Sp
- Dahai Zhang, S. Fukuzawa, K. Tachibana
- Chemistry, BiologyNatural Product Communications
- 1 November 2012
The structures of these compounds were elucidated based on chemical and physicochemical evidence, including MS, UV, IR and NMR spectra, and the stereochemistry of 1 was further confirmed by catalytic reaction of 5 with p-TsOH as a catalyst.