Regioselective Synthesis of 4‐Aryl‐1,3‐dihydroxy‐2‐naphthoates through 1,2‐Aryl‐Migrative Ring Rearrangement Reaction and their Photoluminescence Properties - Normandie Université Access content directly
Journal Articles Chemistry - A European Journal Year : 2021

Regioselective Synthesis of 4‐Aryl‐1,3‐dihydroxy‐2‐naphthoates through 1,2‐Aryl‐Migrative Ring Rearrangement Reaction and their Photoluminescence Properties

Abstract

4-Aryl-1,3-dihydroxy-2-naphthoates having the less accessible 1,2,3,4-tetrasubstituted naphthalene scaffold and that show photoluminescence emission from solid state as well as in solutions, were selectively synthesized from brominated lactol silyl ethers through the 1,2-aryl-migrative ring rearrangement reaction.
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Dates and versions

hal-03361266 , version 1 (23-11-2022)

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Hikaru Yanai, Teru Kawazoe, Nobuyuki Ishii, Bernhard Witulski, Takashi Matsumoto. Regioselective Synthesis of 4‐Aryl‐1,3‐dihydroxy‐2‐naphthoates through 1,2‐Aryl‐Migrative Ring Rearrangement Reaction and their Photoluminescence Properties. Chemistry - A European Journal, 2021, 27 (44), pp.11442-11449. ⟨10.1002/chem.202101459⟩. ⟨hal-03361266⟩
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