Prymnesin-2: A potent ichthyotoxic and hemolytic glycoside isolated from the red tide alga Prymnesium parvum
Igarashi T, Satake M, Yasumoto T. Prymnesin-2: a potent ichthyotoxic and hemolytic glycoside isolated from the red tide alga Prymnesium parvum. J Am Chem Soc 1996;118:479-480.
Structures and partial stereochemical assignments for prymnesin-1 and prymnesin-2: Potent hemolytic and ichthyotoxic glycosides isolated from the red tide alga Prymnesium parvum
Igarashi T, Satake M, Yasumoto T. Structures and partial stereochemical assignments for prymnesin-1 and prymnesin-2: potent hemolytic and ichthyotoxic glycosides isolated from the red tide alga Prymnesium parvum. J Am Chem Soc 1999;121:8499-8511.
Long-range carbon-proton coupling constants for stereochemical assignment of acyclic structures in natural products: Configuration of the C5-C9 portion of matotoxin
Matsumori N, Nonomura T, Sasaki M, Murata M, Tachibana K, Satake M, Yasumoto T. Long-range carbon-proton coupling constants for stereochemical assignment of acyclic structures in natural products: configuration of the C5-C9 portion of matotoxin. Tetrahedron Lett 1996;37:1269-1272.
New chiral anisotropic reagents, NMR tools to elucidate the absolute configurations of long-chain organic compounds
Kusumi T, Takahashi H, Xu P, Fukushima T, Asakawa Y, Hashimoto T, Kan Y, Inouye Y. New chiral anisotropic reagents, NMR tools to elucidate the absolute configurations of long-chain organic compounds. Tetrahedron Lett 1994;35:4397-4400.
A fluorometric determination method for D,L configurations of per-O-methylated monosaccharides by anomeric 2-methyl-2-β-naphthyl-1,3-benzodioxole-4-carboxylation and high-performance liquid chromatography
Bai C. Ohrui H, Nishida Y, Meguro H. A fluorometric determination method for D,L configurations of per-O-methylated monosaccharides by anomeric 2-methyl-2-β-naphthyl-1,3-benzodioxole-4-carboxylation and high-performance liquid chromatography. Anal Biochem 1997;246:246-252.
On the use of O-methylmandelic acid for the establishment of absolute configuration of α-chiral primary amines
Trost BM, Bunt RC, Pulley SR. On the use of O-methylmandelic acid for the establishment of absolute configuration of α-chiral primary amines. J Org Chem 1994;59:4202-4205.