One‐Pot Access to Sulfonyl 2‐Arylnaphthalenes via Wacker Oxidation of Sulfonyl  o ‐Allylchalcones | Zendy

Hsueh NaiChen | Zendy; Tsai MinChen | Zendy; Chang MengYang | Zendy

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One‐Pot Access to Sulfonyl 2‐Arylnaphthalenes via Wacker Oxidation of Sulfonyl o ‐Allylchalcones

Author(s) -

Hsueh NaiChen,

Tsai MinChen,

Chang MengYang

Publication year - 2020

Publication title -

advanced synthesis and catalysis

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.541

H-Index - 155

eISSN - 1615-4169

pISSN - 1615-4150

DOI - 10.1002/adsc.202000868

Subject(s) - chemistry , sulfonyl , intramolecular force , ring (chemistry) , wacker process , medicinal chemistry , yield (engineering) , carbon fibers , catalysis , combinatorial chemistry , organic chemistry , photochemistry , ethylene , alkyl , materials science , composite number , metallurgy , composite material

Under the oxygen atmosphere conditions, PdCl 2 /CuCl 2 ‐mediated one‐pot Wacker‐type decarboxylative benzannulation of sulfonyl o ‐allylchalcones provides sulfonyl naphthalenes and carboxylic acids in MeOH at reflux. A plausible mechanism is proposed and discussed herein. This high‐yield protocol provides a highly effective intramolecular ring‐closure via one carbon‐carbon double bond (C=C) formation.

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