Web4 Oct 2012 · Remote anionic Fries rearrangement of sulfonates: regioselective synthesis of indole triflones. Xiuhua Xu, Misaki Taniguchi, Ayaka Azuma, Guokai Liu, Etsuko Tokunaga, … WebThe direct conversion of a phenolic hydroxyl group into a free amino group is a useful method for the preparation of primary aryl amines that are hard to synthesize by using coupling reactions involving phenol derivatives with ammonia. Whereas reactions of ortho‐ and meta‐substituted phenols produced meta‐substituted anilines exclusively, th…
Thia-Fries rearrangement of aryl triflinates to ... - ScienceDirect
WebThe Fries rearrangement reaction is an organic name reaction which involves the conversion of phenolic esters into hydroxyaryl ketones on heating in the presence of a catalyst. … Web7 Apr 2024 · Fries rearrangement reaction is necessary for the production of ortho-acyl hydroxy 2.2 paracyclophanes, which has significant industrial importance. In the medical … send a file to my kindle
One‐Pot Generation of Benzynes from Phenols: Formation of …
Web9 Jul 2013 · In contrast to Lloyd-Jones' reaction system in the cryogenic regime, where thia-Fries rearrangement was orthogonal to aryne generation depending on reaction … WebThe remarkable feature of new precursors is the selective generation of 3-haloarynes by suppressing the competitive thia-Fries rearrangement, which is the problem in the … Web1 Sep 2003 · Remote anionic Fries rearrangement of sulfonates: regioselective synthesis of indole triflones. An unusual NaH-mediated remote anionic 1,5-thia-Fries rearrangement … send a fish black friday