158670-19-0Relevant articles and documents
Palladium-catalyzed C-3 desulfitative arylation of indolizines with sodium arylsulfinates and arylsulfonyl hydrazides
Wang, Chunjie,Jia, Huali,Li, Zhiwei,Zhang, Hui,Zhao, Baoli
, p. 21814 - 21821 (2016/03/08)
Derivatized indolizines were efficiently prepared by direct C-3 arylation of indolizines using sodium arylsulfinates and arylsulfonyl hydrazides. Pd-catalyzed desulfitative C-3 arylation with sodium arylsulfinates was achieved with the assistance of peroxides, and the catalytic efficiency was promoted by N-containing ligands. Arylsulfonyl hydrazides were also successfully applied in Pd-catalyzed desulfitative C-3 arylation with indolizines, and the side homocoupling reactions can be restrained in the component solvent under milder conditions. Various derivatives were synthesized in good yields by both methods, offering expedient protocols for the synthesis of C-3 functionalized indolizine molecules.
Formation of Indolizines by the Addition of α-Chloroacrylonitrile to Pyridinium Ylides: Regioselectivity and Hammett Correlation
Bonneau, Roland,Liu, Michael T. H.,Lapouyade, Rene
, p. 1547 - 1548 (2007/10/02)
Cycloaddition of pyridinium ylides to α-chloroacrylonitrile give indolizines: the regioselectivity of the reaction can be rationalized in terms of nucleophilic attack by the ylides on the olefin.
