58812-72-9Relevant articles and documents
A unified approach to sesquiterpenes sharing trimethyl(p-tolyl) cyclopentanes: Formal total synthesis of (±)-laurokamurene B
Das, Mrinal K.,Dinda, Bidyut K.,Bisai, Vishnumaya
, p. 2039 - 2042 (2019/07/08)
A unified approach to the sesquiterpenoids sharing common trimethyl(p-tolyl) cyclopentane skeleton has been disclosed via a key Stork-Danheiser sequence on a cyclopentane based vinylogous ester with aryl Grignard reagent followed by α-methylation strategy
Novel synthetic approach toward (±)-β-cuparenone via palladium-catalyzed tandem Heck cyclization of 1-bromo-5-methyl-1-aryl-hexa-1,5- dien-3-ol derivatives
Ray, Devalina,Ray, Jayanta K.
, p. 191 - 194 (2007/10/03)
(Chemical Equation Presented) A novel and convenient synthetic route toward (±)-β-cuparenone and many other sesquiterpene natural product precursors has been developed via palladium-catalyzed tandem Heck cyclization of 1-bromo-5-methyl-1-aryl-hexa-1,5-die
Acid-catalysed Thermal Rearrangement of γ,δ-Unsaturated Ketones
Srikrishna, Adusumilli,Krishnan, Kathiresan,Vankateswarlu, Somepalli
, p. 143 - 145 (2007/10/02)
Thermal activation of γ,δ-unsaturated ketones (1, 9 and 12) in the presence of a catalytic amount of propionic acid causes a rearrangement to give new γ,δ-unsaturated ketones (2, 10 and 14) via an intramolecular ene reaction followed by a retro-ene reacti