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Benzylic Phosphates in Friedel–Crafts Reactions with Activated and Unactivated Arenes: Access to Polyarylated Alkanes

Version 3 2016-04-13, 16:19
Version 2 2016-02-29, 13:49
Version 1 2016-02-16, 13:48
Posted on 2016-03-04 - 00:00
Easily reachable electron-poor/rich primary and secondary benzylic phosphates are suitably used as substrates for Friedel–Crafts benzylation reactions with only 1.2 equiv activated/deactivated arenes (no additional solvent) to access structurally and electronically diverse polyarylated alkanes with excellent yields and selectivities at room temperature. Specifically, diversely substituted di/triarylmethanes are generated within 2–30 min using this approach. A wide number of electron-poor polyarylated alkanes are easily accomplished through this route by just tuning the phosphates.

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