Yang, Pusu; Liu, Chenxu; Zhang, Wenwen; You, Shuli published an article in 2021, the title of the article was Ir-catalyzed enantioselective Friedel-Crafts type allylic substitution of indolizines.Category: esters-buliding-blocks And the article contains the following content:
Indolizine is an important N-containing heterocyclic nucleus and their derivatives display interesting biol. activities. The development of synthetic methods towards indolizine derivatives has attracted extensive attention. Despite the rapid growth in this area, asym. synthesis of indolizine derivatives has been rarely reported. Ir-catalyzed asym. allylic substitution reaction is an efficient method for the enantioselective construction of C-C or C-X bonds, furnishing terminal olefins bearing a stereogenic center at the allylic position with excellent regio- and enantioselectivities. In this regard, various electron-rich arenes, including indoles, pyrroles, naphthols, have been applied as the nucleophiles via Friedel-Crafts type process in the allylic substitution reactions. As a class of constitutional isomers of indoles, indolizines are now demonstrated as suitable nucleophiles in transition-metal-catalyzed allylic substitution reactions. Herein, an iridium- catalyzed enantioselective allylic substitution of allylic alc. with indolizine is reported. A broad range of 3-allylindolizines were accessed with high yields (83%∼95%) and excellent enantioselectivities (95%∼>99% ee). A general procedure for the asym. allylation of indolizines is described in the following: A flame-dried Schlenk tube was cooled to room temperature and filled with argon. To this flask were added [Ir(cod)Cl]2 (4.0 mg, 0.006 mmol, 3 mol%) and (S)-L1 (12.1 mg, 0.024 mmol, 12 mol%). After the flask was evacuated and refilled with argon for three times, freshly distilled dichloromethane (DCM) (2 mL) were added. After the mixture was stirred for 15 min at room temperature, indolizines (0.2 mmol, 1.0 equivalent), allylic alcs. (0.4 mmol, 2.0 equivalent) and (PhSO2)2 NH (18.0 mg, 0.06 mmol, 30 mol%) were added under argon atm. The reaction mixture was stirred at room temperature and monitored by thin-layer chromatog. (TLC). Once indolizines were consumed, the reaction was diluted with water (5 mL), and the mixture was extracted with EtOAc (10 mL×3). The organic layer was collected, dried over Na2SO4 and then concentrated in vacuo to afford the crude product. This crude material was purified by column chromatog. to afford the product. The experimental process involved the reaction of Ethyl indolizine-1-carboxylate(cas: 93476-46-1).Category: esters-buliding-blocks
The Article related to iridium catalyst enantioselective friedel crafts allylic substitution indolizine, Heterocyclic Compounds (One Hetero Atom): Indoles, Indolizines, Carbazoles, and Other Arenopyrroles and other aspects.Category: esters-buliding-blocks
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