30557-76-7Relevant academic research and scientific papers
ASYMMETRIC MICHAEL ADDITION OF A CHIRAL ESTER-DIENOLATE: ENANTIOSELECTIVE SYNTHESIS OF (-)-KHUSIMONE
Oppolzer, Wolfgang,Pitteloud, Rita,Bernardinelli, Gerald,Baettig, Kurt
, p. 4975 - 4978 (1983)
A double ?-face-selective aprotic Michael addition of the lithium dienolate derived from the chiral senecioate 2b to cyclopentenone coupled with recovery of the auxiliary 14 serves for the enantioselective synthesis of (-)-khusimone 12 (Schemes 1 and 4).
NOVEL METHOD FOR THE SYNTHESIS OF KHUSIMONE
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Paragraph 0042; 0043; 0044; 0045; 0046, (2016/10/20)
A novel method for synthesis of khusimone, by bringing zizanal into contact with an oxidizing reagent in the presence of a base and an organic solvent.
A NEW SYNTHESIS OF (-)-KHUSIMONE
Sakurai, Kazutoshi,Kitahara, Takeshi,Mori, Kenji
, p. 6581 - 6588 (2007/10/02)
(-)-Khusimone 1, the minor essential component of vetiver oil with insect repellent activity, was synthesized starting from (S)-6,6-dimethyl-5-methoxycarbonylmethyl-2-cyclohexen-1-one 2.Lewis acid-catalyzed Diels-Alder reaction was employed to obtain the
Total synthesis of zizaane sesquiterpenes: (-)-khusimone, (+)-zizanoic acid, and (-)-epizizanoic acid
Liu, Hsing-Jang,Chan, Wing Hong
, p. 1081 - 1091 (2007/10/02)
Three sesquiterpenes of the zizaane family, khusimone (1), epizizanoic acid (3), and zizanoic acid (2) have been synthesized in optically active form from the ammonium salt of (-)-l-10-camphorsulfonic acid in sixteen, nineteen, and twenty steps respectively.
