386743-16-4Relevant academic research and scientific papers
Efficient total synthesis of dysidenin, dysidin, and barbamide
Ilardi, Elizabeth A.,Zakarian, Armen
supporting information; experimental part, p. 2260 - 2263 (2012/06/30)
The total syntheses of three trichloroleucine-derived marine natural products-dysidenin, dysidin, and barbamide-capitalized on a practical and highly diastereoselective ruthenium catalyzed radical chloroalkylation of N-acyloxazolidinones as the key step. Copyright
Synthesis of the marine natural product barbamide
Nguyen,Willis,Gerwick
, p. 1934 - 1935 (2007/10/03)
The first total synthesis of the trichlorinated natural product barbamide is described. The convergent approach involves coupling (S)-3-trichloromethylbutanoyl chloride with Meldrum's acid (2,2-dimethyl-1,3-dioxane-4,6-dione) to give 15 followed by additi
