396102-32-2Relevant articles and documents
Total synthesis of (±)-herbertenediol
Srikrishna,Satyanarayana
, p. 2892 - 2900 (2007/10/03)
A formal total synthesis of the sesquiterpene (±)-herbertenediol and its dimers mastigophorenes A-D has been accomplished, starting from vanillin via 2,3-dimethoxy-5-methylbenzaldehyde. A combination of Claisen rearrangement and ring-closing metathesis reactions were employed for the generation of the two vicinal quaternary carbons on a cyclopentane ring.
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