84051-31-0Relevant articles and documents
Asymmetric synthesis of dihydroartemisinic acid through intramolecular Stetter reaction
Rej, Rohan Kalyan,Acharyya, Ranjan Kumar,Nanda, Samik
, p. 4931 - 4937 (2016/07/19)
A short and concise formal synthesis of enantiopure dihydroartemisinic acid from (R)-citronellal is described in this article. Intramolecular version of asymmetric Stetter reaction using Rovis aminoindane based NHC catalyst was explored to access the core
Pheromone syntheses: A tropical approach. Enantioselective synthesis of the (2R,6S,10S) and (2S,6S,10S) isomers of methyl 2,6,10-trimethyldodecanoate
Ferreira, J. Tercio B.,Zarbin, Paulo H. G.
, p. 381 - 388 (2007/10/03)
The enantioselective syntheses of two stereoisomers, (2R,6S,10S) and (2S,6S,10S), of methyl 2,6,10-trimethyldodecanoate, out of eight possible isomers, are described, employing the stereoselective hydroboration of (-)-isopulegol (2) and (+)-neo-isopulegol
ANTIMALARIAL ARTEMISININ ANALOGS: SYNTHESIS OF 2,3-DESETHANO-12-DEOXOARTEMISININ-RELATED COMPOUNDS
Imakura, Yasuhiro,Hachiya, Katsutoshi,Ikemoto, Tomomi,Kabayashi, Shigeru,Yamashita, Shinsuke,et al.
, p. 2125 - 2129 (2007/10/02)
2,3-Desethano-12-deoxoartemisinin-related compounds ((+)-16a) and ((-)-16b) have been synthesized from R-(+)-citronellal (7) by a stereoselective manner, which is applied to the synthesis of various novel antimalarial artemisinin analogs.