1361229-29-9Relevant academic research and scientific papers
Asymmetric synthesis of (+)-tanikolide and the β-methyl-substituted analogues of (+)-tanikolide and (-)-malyngolide
Doran, Robert,Duggan, Lesley,Singh, Surrendra,Duffy, Colm D.,Guiry, Patrick J.
, p. 7097 - 7106 (2012/01/03)
The δ-lactone-containing natural product (+)-tanikolide, a brine shrimp toxin and antifungal compound, was synthesized in nine steps with an overall yield of 26.4 % by employing Sharpless asymmetric epoxidation and ZrCl4-catalyzed intramolecula
