111466-32-1Relevant academic research and scientific papers
Total synthesis of (-)-dactylynes
Gao, Lian-Xun,Murai, Akio
, p. 745 - 774 (2007/10/03)
The first total synthesis of (-)-dactylyne (1) and (-)-isodactylyne (2), which have been isolated from sea hare, is described in detail. Critical steps in the synthesis include a stereoselective construction as well as an intramolecular ring closure of 32, and the effective double elongation reactions (59 → 63 and 64, 67 → 68, and 70 → 71).
Enantioselective Routes toward 1β-Methylcarbapenems from Chiral Aziridines
Tanner, David,He, Hua Ming
, p. 6079 - 6086 (2007/10/02)
This paper describes two enantioselective aziridine-based routes toward 1β-methylthienamycin, 2, and related carbapenems, the key steps being completely regioselective ring-opening reactions of the chiral aziridines 7 and 10 with AlMe3. - Key Words: 1β-me
