95851-72-2Relevant academic research and scientific papers
SYNTHESIS OF MACROCYCLIC TERPENOIDS BY INTRAMOLECULAR CYCLIZATION IX. TOTAL SYNTHESIS OF (+/-)-OBSCURONATIN AND (+)-BIFLORA-4,10(19),15-TRIENE.
Kodama, Mitsuaki,Okumura, Kunihito,Kobayashi, Yoshihisa,Tsunoda, Tetsuto,Ito, Sho
, p. 5781 - 5784 (2007/10/02)
Stereoselective total synthesis of (+/-)-obscuronatin, a marine diterpene with a 10-membered ring, has been achieved utilizing the anion-induced cyclization of an acyclic epoxy sulfide.The synthesis confirmed the stereostructure of the natural product.
