203063-47-2Relevant academic research and scientific papers
Stereoselective construction of the key intermediate for the synthesis of the tetrahydropyranyl antifungal agents (+)-restricticin and (+)-lanomycin
Honda, Toshio,Satoh, Akiko,Yamada, Toshio,Hayakawa, Tomohisa,Kanai, Kazuo
, p. 397 - 405 (2007/10/03)
Stereoselective construction of the key intermediate for the synthesis of naturally occurring antifungal agents, such as (+)-restricticin and (+)-lanomycin, has been achieved by employing a chelation-controlled aldol reaction of methyl α-methyltetronate w
