Lewis Acid-catalyzed [3 + 2]Cyclo-addition of Alkynes with N-Tosyl-aziridines via Carbon–Carbon Bond Cleavage: Synthesis of Highly Substituted 3-Pyrrolines
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https://figshare.com/articles/dataset/Lewis_Acid_catalyzed_3_2_Cyclo_addition_of_Alkynes_with_i_N_i_Tosyl_aziridines_via_Carbon_Carbon_Bond_Cleavage_Synthesis_of_Highly_Substituted_3_Pyrrolines/2582422
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资源简介：
A novel, efficient, and highly regioselective Lewis acid-catalyzed [3 + 2] cycloaddition of alkynes with azomethine ylides, which are easily obtained from N-tosylaziridines via C–C bond heterolysis at room temperature was developed. Moderate enantioselectivity (70% ee) can be achieved by the application of the commercially available chiral Pybox 7 as the ligand.
创建时间：
2016-02-22
