Catalytic, regioselective Friedel–Crafts alkylation of beta-naphthol-Reference-Cited by-同舟云学术

Catalytic, regioselective Friedel–Crafts alkylation of beta-naphthol

Published:2024 Issue:10 Volume:48 Page:4224-4228
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Ash Jeffrey¹,Ahmed Emarose¹,Le Ngantu¹,Huang Hai²^ORCID,Kang Jun Yong¹^ORCID

Affiliation:

1. Department of Chemistry and Biochemistry, University of Nevada Las Vegas, 4505 S. Maryland Parkway, Las Vegas, Nevada, 89154-4003, USA

2. Jiangsu Key Laboratory of Advanced Catalytic Materials & Technology, School of Petrochemical Engineering, Changzhou University, Changzhou, 213164, P. R. China

Abstract

A catalytic, regioselective, and atom-economic Friedel–Crafts alkylation reaction of beta-naphthol using allylic alcohols has demonstrated functionalized naphthol synthesis under mild reaction conditions.

Funder

University of Nevada, Las Vegas

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/NJ/D3NJ05580A

Reference63 articles.

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3. Naproxen derivatives: Synthesis, reactions, and biological applications

4. BINOLs as visible light photocatalysts for metal-free atom transfer radical polymerization

5. Binaphthol-derived phosphoric acid as a versatile catalyst for enantioselective carbon–carbon bond forming reactions

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