50906-52-0Relevant articles and documents
A stereoselective total synthesis of (±)-oppositol by a doubly diastereoselective intramolecular ester enolate alkylation
Kim, Deukjoon,Kim, In Ho
, p. 415 - 416 (2007/10/03)
The brominated terpene (±)-oppositol (1) has been synthesized utilizing a novel doubly diastereodifferentialing 'folding and allylic strain-controlled' intramolecular ester enolate alkylation.
SYNTHESIS OF (+/-)-PREPINNATERPENE, A BROMODITERPENE FROM THE RED ALGA LAURENCIA PINNATA YAMADA
Fukuzawa, Akio,Sato, Hideaki,Masamune, Tadashi
, p. 4303 - 4306 (2007/10/02)
A total synthesis of (+/-)-prepinnaterpene, a brominated diterpene with a unique skeleton, and (+/-)-oppositol, a related sesquiterpene, is described.
BIOMIMETIC SYNTHESES OF OPPOSITOL, OPLOPANONE, AND APHANAMOL II FROM GERMACRENE-D
Shizuri, Yoshikazu,Shu, Yamaguchi,Terada, Yukimasa,Yamamura, Shosuke
, p. 57 - 60 (2007/10/02)
Biomimetic reaction of germacrene-D induced with bromonium ion has been carried out to give several bromo compounds, from which (+/-)-oppositol and (+/-)-oplopanone have been synthesized. (+/-)-Aphanamol II has also been synthesized from epoxygermacrene-D.