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- W2639942923 abstract "A class of multifunctional amidophosphanes derived from chiral α-amino acids have been developed with two amide bonds, a tertiary amine and a phosphine. In combination with Ag(I) salts, these amidophosphanes have been demonstrated as highly efficient multifunctional catalysts in the asymmetric 1,3-dipolar cycloaddition of azomethine ylides as well as the three-component reaction of the α-iminoesters in situ generated. Under optimal conditions, highly functionalized endo-8 pyrrolidines were obtained with good to excellent yields (up to 99% yield) and enantioselectivities (up to 98% ee)." @default.
- W2639942923 created "2017-06-30" @default.
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- W2639942923 date "2017-07-01" @default.
- W2639942923 modified "2023-10-14" @default.
- W2639942923 title "A class of α-amino acids-derived multifunctional amidophosphane precatalysts: application to the highly enantio- and diastereoselective silver(I)-catalyzed 1,3-dipolar cycloaddition reaction" @default.
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- W2639942923 doi "https://doi.org/10.1016/j.tetasy.2017.05.014" @default.
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