71357-60-3Relevant articles and documents
Total synthesis of (±)-joubertinamine from 3-(3,4-dimethoxyphenyl)- 5-bromo-2-pyrone
Tam, Nguyen Thanh,Cho, Cheon-Gyu
, p. 3391 - 3392 (2008/02/12)
The regioselective synthesis and Diels-Alder cycloaddition of 3-(3,4-dimethoxyphenyl)-5-bromo-2-pyrone provided a new efficient synthetic route to joubertinamine (9.6% total yield over 10 steps).
A Synthesis of Seco-mesembrane Alkaloids, (+/-)-Joubertiamine, (+/-)-Joubertinamine, and (+/-)-Epijoubertinamine
Hoshino, Osamu,Ishizaki, Miyuki,Sawaki, Shohei,Yuasa, Masayuki,Umezawa, Bunsuke
, p. 3373 - 3380 (2007/10/02)
A synthesis of seco-mesembrane alkaloids, (+/-)-joubertiamine (4), (+/-)-joubertinamine (5), and (+/-)-epijoubertinamine (6), was accomplished starting with 2-allyl-2-aryl-5,5-ethylenedioxycyclohexanones (10 and 3), which are readily available by allylati
Total Syntheses of (+/-)-Mesembrine, (+/-)-Joubertinamine, and (+/-)-N-Demethylmesembrenone
Jeffs, Peter, W.,Redfearn, Richard,Wolfram, Joachim
, p. 3861 - 3863 (2007/10/02)
The syntheses of three members of the sceletium alkaloid family are developed from a common synthon, leading to short, high-yielding stereorational routes to (+/-)-mesembrine, (+/-)-joubertinamine, and (+/-)-N-demethylmesembrenone.The latter is synthesize