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ChemInform Abstract: Structures and Partial Stereochemical Assignments for Prymnesin-1 and Prymnesin-2: Potent Hemolytic and Ichthyotoxic Glycosides Isolated from the Red Tide Alga Prymnesium parvum.

โœ Scribed by Tomoji Igarashi; Masayuki Satake; Takeshi Yasumoto


Publisher
John Wiley and Sons
Year
2010
Weight
25 KB
Volume
31
Category
Article
ISSN
0931-7597

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Synthesis and stereochemical confirmatio
โœ Makoto Sasaki; Takeshi Shida; Kazuo Tachibana ๐Ÿ“‚ Article ๐Ÿ“… 2001 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 152 KB

Stereocontrolled synthesis of the HI/JK ring model of the prymnesins, glyosidic toxins isolated from the red tide phytoflagellate Prymnesium parvum, is described. Comparison of its 1 H and 13 C NMR data with those of the natural toxins established the earlier stereochemical assignments.