1619902-16-7Relevant academic research and scientific papers
Synthesis of four diastereomers and structural revision of tetradenolide
Tokuda, Maki,Kurogome, Yuji,Katoh, Rieko,Nohara, Yukie,Hattori, Yasunao,Makabe, Hidefumi
, p. 4189 - 4192 (2014/07/22)
Four diastereomers of tetradenolide, a cytotoxic α-pyrone isolated from Tetradenia riparia, were synthesized stereoselectively using the Z-selective Horner-Emmons reaction followed by acid catalyzed lactonization. Making comparison of the 1H an
