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- W2897024212 abstract "The asymmetric allylation of 1-pyrroline-5-carboxylic esters has been accomplished through a synergistic Pd/Cu catalyst system under mild reaction conditions. The mechanistic studies suggested that (1) nucleophilic attack is the enantiodiscriminating step; (2) the cooperative action of two chiral reactive species, N-metalated azomethine ylides and π-allylpalladium, is most likely responsible for its high reactivity and excellent enantioselectivity (up to >99% ee); and (3) the steric hindrance and electronic factors of the allylic electrophiles and imino ester substrates are crucial for the formation of the linear products. A series of 3,4-2 H-pyrrole derivatives bearing a quaternary stereogenic center were easily synthesized in high yields and with high to excellent regioselectivity and enantioselectivity." @default.
- W2897024212 created "2018-10-26" @default.
- W2897024212 creator A5043883660 @default.
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- W2897024212 creator A5082306289 @default.
- W2897024212 date "2018-10-10" @default.
- W2897024212 modified "2023-10-16" @default.
- W2897024212 title "Stereoselective Allylic Alkylation of 1-Pyrroline-5-carboxylic Esters via a Pd/Cu Dual Catalysis" @default.
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- W2897024212 doi "https://doi.org/10.1021/acs.orglett.8b02902" @default.
- W2897024212 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30303386" @default.
- W2897024212 hasPublicationYear "2018" @default.
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