Helvetica Chimica Acta p. 480 - 486 (1992)
Update date:2022-08-16
Topics:
Baumgarner, Charles D.
Malen, Alyssa H.
Pastor, Stephen D.
NabiRahni, M. Ali
The reaction of 9-bromoanthracene (1) with benzenethiol(ate) in tetraglyme proceeds by a SNAr mechanism.The concurrent formation of anthracene is not due to a competing single-electron-transfer pathway involving either benzenethiol or benzenethiolate anion.
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