Tetrahedron Letters p. 5781 - 5784 (1984)
Update date:2022-08-03
Topics:
Kodama, Mitsuaki
Okumura, Kunihito
Kobayashi, Yoshihisa
Tsunoda, Tetsuto
Ito, Sho
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.
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