440361-90-0Relevant academic research and scientific papers
Total synthesis of Sceletium alkaloids (±)-joubertinamine, (±)-epijoubertinamine, (±)-tortuosamine and formal synthesis of (±)-mesembrine, (±)-N-formyltortuosamine
Bhosale, Viraj A.,Ukale, Dattatraya U.,Waghmode, Suresh B.
, p. 9432 - 9440 (2016)
An efficient collective formal/total synthesis of Sceletium alkaloids and their seco-congeners has been reported. The bicyclic core of (±)-mesembrine, (±)-tortuosamine, and (±)-N-formyltortuosamine with all required functionalities including the character
Palladium-catalyzed sequential arylation and allylic alkylation of highly functionalized ketones: A concise synthesis of mesembrine
Zhao, Yuanhong,Zhou, Yongyun,Liang, Leilei,Yang, Xiaodong,Du, Fengxiang,Li, Ang,Zhang, Hongbin
supporting information; experimental part, p. 555 - 558 (2009/07/25)
(Chemical Equation Presented) An unprecedented palladium-catalyzed sequential procedure toward arylation and allylic alkylation of highly functionalized cyclohexenones was developed. This new protocol leads to useful building blocks containing a benzylic
Allyl vinyl ethers via Wittig olefination: A short and efficient synthesis of (±)-mesembrine
Kulkarni, Mukund G.,Rasne, Ravindra M.,Davawala, Saryu I.,Doke, Aniruddha K.
, p. 2297 - 2298 (2007/10/03)
A Wittig olefination-Claisen rearrangement approach has been successfully applied to a short and efficient synthesis of (±)-mesembrine.
