83788-63-0Relevant academic research and scientific papers
A Rapid Route to (+/-)-Herbertene, a New Sesquiterpene
Leriverend, Marie-Louise,Vazeux, Michel
, p. 866 - 867 (1982)
A four-step synthesis of (+/-)-herbertene has been achieved via the regioselective ring enlargement of 2,2,3-trimethyl-3-(m-tolyl)cyclobutanone.
2,2-Dimethyl cyclopentanones by acid catalyzed ring expansion of isopropenylcyclobutanols. A short synthesis of (±)-α-cuparenone and (±)-herbertene
Bernard, Angela M.,Frongia, Angelo,Secci, Francesco,Piras, Pier P.
, p. 3853 - 3855 (2007/10/03)
2,2-Dimethyl cyclopentanones are readily prepared by acid catalyzed ring expansion of isopropenylcyclobutanols; the method allows ready access to the family of sesquiterpenes cuparanes and herbertanes, as demonstrated by the synthesis of (±)-α-cuparenone
A ring closing metathesis-based approach to (±)-herbertene, (±)-α-herbertenol, (±)-β-herbertenol and (±)-herbertenediol
Srikrishna,Rao, M. Srinivasa
, p. 340 - 342 (2007/10/03)
An efficient methodology for the synthesis of the aromatic sesquiterpenes (±)-herbertene, (±)-α-herbertenol, (±)-β-herbertenol (±)-herbertenediol and (±)-α-cuparenone, employing a combination of Claisen rearrangement and ring closing metathesis reactions,
New total synthesis of (±)-herbertene, (±)-β-herbertenol and (±)-herbertenediol
Gupta,Pal,Roy,Mukherjee
, p. 7563 - 7566 (2007/10/03)
The total syntheses of the herbertane sesquiterpenes (±)-herbertene (1), (±)-β-herbertenol (2) and (±)-herbertenediol (5) have been successfully accomplished involving copper-catalysed conjugate addition of Grignard reagents to unsaturated compounds and α
