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- W2891749344 abstract "Abstract A series of 4‐nitrobenzofuroxans were examined in [3+2]‐cycloaddition reactions with N‐benzyl azomethine ylide. The reaction outcome was found to be dependent on the nature of substituent 7‐R: for R=H and SR’ the products of double cycloaddition of the dipole were isolated, whereas for R=CH 3 , OR’ and NR'R” tetrahydroisoindoles annelated with furoxan ring were the sole products. As a result efficient chemoselective method for the synthesis of mono‐ and bis‐pyrrolidine fused benzofuroxan derivatives was developed." @default.
- W2891749344 created "2018-09-27" @default.
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- W2891749344 date "2018-09-10" @default.
- W2891749344 modified "2023-09-26" @default.
- W2891749344 title "Unusual Pericyclic Reactivity of 4-Nitrobenzofuroxans in 1,3-Dipolar Cycloaddition with N-Benzyl Azomethine Ylide - A New Example of Multiple C-C-Bond Forming Transformations." @default.
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- W2891749344 doi "https://doi.org/10.1002/slct.201802117" @default.
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