41955-12-8Relevant academic research and scientific papers
Total Synthesis of the (+)-Antimycin A Family
Inai, Makoto,Nishii, Takeshi,Tanaka, Ayako,Kaku, Hiroto,Horikawa, Mitsuyo,Tsunoda, Tetsuto
, p. 2719 - 2729 (2011/06/23)
An asymmetric aldol reaction using Oppolzer's sultam has provided a practical and efficient synthetic route (15 steps, overall yield ca. 24%) to 12 compounds of the Antimycin A family and deisovalerylblastmycin, which were obtained in pure form on a 60-300 mg scale. In the syntheses, the nine-membered dilactone ring was constructed successfully by lactonization of a 2-pyridinethiol ester bearing a TIPS group on the 8-OH by using the (CuOTf) 2A·PhH complex. An asymmetric aldol reaction usingOppolzer's sultam has provided a practical and efficient synthetic route (15 steps, overall yield ca. 24%) to 12 compounds of the antimycin A family and deisovalerylblastmycin, which were obtained in pure form on a 60-300 mg scale.
Singley oxygen in synthesis. Formation of antimycin A3 from an oxazole template
Wasserman, Harry H.,Gambale, Ronald J.
, p. 7059 - 7070 (2007/10/02)
Antimycin A3 has been synthesized using an oxazole template for constructing the framework of the dilactone. Formation of the nine-membered ring was accomplished by reaction of an ω-hydroxyl group with an activated carboxylate generated in the
