95851-64-2Relevant 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.
Phenyl derivatives
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, (2008/06/13)
Phenyloxy, phenylsulfinyl, phenylthio, phenylsulfonyl, benzyloxy, benzylthio, benzylsulfinyl, or benzylsulfonyl, alkyl or alkenyl derivatives wherein the alkyl or alkenyl group contains at least 7 carbon atoms which are useful in killing and preventing proliferation of insects by upsetting their hormone balance.
