694520-62-2Relevant academic research and scientific papers
Contribution to the total synthesis of caribenolide I
Jalce, Ga?l,Franck, Xavier,Seon-Meniel, Blandine,Hocquemiller, Reynald,Figadère, Bruno
, p. 5905 - 5908 (2006)
Stereoselective synthesis of C13-C29 fragment of caribenolide I, a potent antitumour macrolide isolated from a marine dinoflagellate Amphidinium sp. is described. The key step relies on a highly diastereoselective C-glycosylation, us
Highly Diastereoselective Synthesis of trans-2,5-Disubstituted Tetrahydrofurans
Jalce, Gael,Seck, Matar,Franck, Xavier,Hocquemiller, Reynald,Figadere, Bruno
, p. 3240 - 3241 (2007/10/03)
trans-2,5-Disubstituted tetrahydrofurans were obtained as major diastereomers (trans / cis ratio 90:10-100: 0) when acetylated y-lactols derived from (S)-glutamic acid were treated with titanium enolates of N-acetyl (R)-oxazolidin-2-thiones. A simple tran
