Benzylic Phosphates
in Friedel–Crafts Reactions
with Activated and Unactivated Arenes: Access to Polyarylated Alkanes
Version 3 2016-04-13, 16:19Version 3 2016-04-13, 16:19
Version 2 2016-02-29, 13:49Version 2 2016-02-29, 13:49
Version 1 2016-02-16, 13:48Version 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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Pallikonda, Gangaram; Chakravarty, Manab (2016). Benzylic Phosphates
in Friedel–Crafts Reactions
with Activated and Unactivated Arenes: Access to Polyarylated Alkanes. ACS Publications. Collection. https://doi.org/10.1021/acs.joc.5b02441