343239-55-4Relevant articles and documents
Protecting group free formal total synthesis of the antitubercular agent erogorgiaene
Yadav, Jhillu S.,Thirupathaiah, Bodakuntla,Al Khazim Al Ghamdi, Ahmad
, p. 2072 - 2076 (2012)
The formal total synthesis of the antitubercular agent erogorgiaene was achieved in 12 steps by using a protecting group free strategy. The synthesis involves an enamine-mediated 1,4-addition, an aldol condensation, dehydrogenation, Wittig olefination, in
Identification, synthesis, and bioassay of a male-specific aggregation pheromone from the harlequin bug, Murgantia histrionica
Zahn, Deane K.,Moreira, Jardel A.,Millar, Jocelyn G.
, p. 238 - 251 (2008/09/17)
Sexually mature male harlequin bugs produced a sex-specific compound, identified as one of the stereoisomers of the sesquiterpene epoxyalcohol 4-[3-(3,3-dimethyloxiran-2-yl)-1-methylpropyl]-1-methylcyclohex-2-en-1-ol (henceforth murgantiol), a compound wi
Total synthesis of bisabolane sesquiterpenoids, α-bisabol-1-one, curcumene, curcuphenol and elvirol: Utility of catalytic enamine reaction in cyclohexenone synthesis
Hagiwara, Hisahiro,Okabe, Tomoyuki,Ono, Hiroki,Kamat, Vijayendra P.,Hoshi, Takashi,Suzuki, Toshio,Ando, Masayoshi
, p. 895 - 900 (2007/10/03)
Total syntheses of α-bisabol-1-one, curcumene, curcuphenol and elvirol have been accomplished via 1,4-conjugate addition of intact aldehydes to vinyl ketones followed by an intramolecular aldol condensation.