308101-29-3Relevant academic research and scientific papers
Enantioselective Synthesis of 3-Allylindolizines via Sequential Rh-Catalyzed Asymmetric Allylation and Tschitschibabin Reaction
Li, Ke,Li, Changkun
supporting information, p. 9456 - 9461 (2020/12/21)
The first highly regio- and enantioselective synthesis of 3-allylindolizines has been developed by the sequential Rh-catalyzed asymmetric allylation and Tschitschibabin reaction. Above the 20:1 branch/linear ratio, up to a 96% yield and 99% ee could be obtained with the help of tert-butyl-substituted chiral bisoxazolinephosphine ligand. In situ generated highly nucleophilic 2-alkylpyridinium ylides are utilized to undergo the asymmetric alkylation reaction before cyclization.
A Practical Parallel Synthesis of 2-Substituted Indolizines
Chai, Wenying,Kwok, Annette,Wong, Victoria,Carruthers, Nicholas I.,Wu, Jiejun
, p. 2086 - 2088 (2007/10/03)
A practical parallel synthesis of 2-substituted indolizines 4 via phase-separation techniques is reported. Their further transformation into indolizidines 5 is also described.
