An improved synthesis of (-)-5,11-dideoxytetrodotoxin. 2013

Masaatsu Adachi, and Takuya Imazu, and Minoru Isobe, and Toshio Nishikawa
Laboratory of Organic Chemistry, Graduate School of Bioagricultural Sciences, Nagoya University, Chikusa, Nagoya 464-8601, Japan.

We describe an improved synthesis of (-)-5,11-dideoxytetrodotoxin from an enone, which was used for synthesis of tetrodotoxin and its analogues in this laboratory. One of the major modifications was to establish a two-step guanidinylation of trichloroacetamide of a highly functionalized intermediate, which allowed us to prepare (15)N(2)-labeled 5,11-dideoxytetrodotoxin for biosynthetic investigations.

UI MeSH Term Description Entries
D000081 Acetamides Derivatives of acetamide that are used as solvents, as mild irritants, and in organic synthesis.
D013237 Stereoisomerism The phenomenon whereby compounds whose molecules have the same number and kind of atoms and the same atomic arrangement, but differ in their spatial relationships. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed) Molecular Stereochemistry,Stereoisomers,Stereochemistry, Molecular,Stereoisomer
D013779 Tetrodotoxin An aminoperhydroquinazoline poison found mainly in the liver and ovaries of fishes in the order TETRAODONTIFORMES, which are eaten. The toxin causes paresthesia and paralysis through interference with neuromuscular conduction. Fugu Toxin,Tarichatoxin,Tetradotoxin,Toxin, Fugu
D015394 Molecular Structure The location of the atoms, groups or ions relative to one another in a molecule, as well as the number, type and location of covalent bonds. Structure, Molecular,Molecular Structures,Structures, Molecular
D019791 Guanidine A strong organic base existing primarily as guanidium ions at physiological pH. It is found in the urine as a normal product of protein metabolism. It is also used in laboratory research as a protein denaturant. (From Martindale, the Extra Pharmacopoeia, 30th ed and Merck Index, 12th ed) It is also used in the treatment of myasthenia and as a fluorescent probe in HPLC. Guanidine Hydrochloride,Guanidinium,Guanidinium Chloride,Guanidine Monohydrate,Guanidine Monohydrobromide,Guanidine Monohydrochloride,Guanidine Monohydroiodine,Guanidine Nitrate,Guanidine Phosphate,Guanidine Sulfate,Guanidine Sulfate (1:1),Guanidine Sulfate (2:1),Guanidine Sulfite (1:1),Guanidium Chloride,Chloride, Guanidinium,Chloride, Guanidium,Hydrochloride, Guanidine,Monohydrate, Guanidine,Monohydrobromide, Guanidine,Monohydrochloride, Guanidine,Monohydroiodine, Guanidine,Nitrate, Guanidine,Phosphate, Guanidine,Sulfate, Guanidine
D062845 Chloroacetates ACETIC ACID or acetic acid esters substituted with one or more CHLORINE atoms. Chloroacetic Acids,Acids, Chloroacetic

Related Publications

Masaatsu Adachi, and Takuya Imazu, and Minoru Isobe, and Toshio Nishikawa
October 1999, Angewandte Chemie (International ed. in English),
Masaatsu Adachi, and Takuya Imazu, and Minoru Isobe, and Toshio Nishikawa
January 2004, Chemistry (Weinheim an der Bergstrasse, Germany),
Masaatsu Adachi, and Takuya Imazu, and Minoru Isobe, and Toshio Nishikawa
August 2002, Organic letters,
Masaatsu Adachi, and Takuya Imazu, and Minoru Isobe, and Toshio Nishikawa
February 1991, Journal of medicinal chemistry,
Masaatsu Adachi, and Takuya Imazu, and Minoru Isobe, and Toshio Nishikawa
September 1981, Journal of medicinal chemistry,
Masaatsu Adachi, and Takuya Imazu, and Minoru Isobe, and Toshio Nishikawa
May 1979, Experientia,
Masaatsu Adachi, and Takuya Imazu, and Minoru Isobe, and Toshio Nishikawa
March 1975, Journal of medicinal chemistry,
Masaatsu Adachi, and Takuya Imazu, and Minoru Isobe, and Toshio Nishikawa
December 1984, Journal of pharmaceutical sciences,
Masaatsu Adachi, and Takuya Imazu, and Minoru Isobe, and Toshio Nishikawa
October 1960, Biochimica et biophysica acta,
Masaatsu Adachi, and Takuya Imazu, and Minoru Isobe, and Toshio Nishikawa
November 1976, The Journal of organic chemistry,
Copied contents to your clipboard!