A Facile Access to 4-Substituted-2-naphthols via a Tandem Friedel–Crafts Reaction: A β-Chlorovinyl Ketone Pathway
Author:
Affiliation:
1. College of Pharmacy, Chung-Ang University, 84 Heukseok-ro, Dongjak, Seoul 156-756, Republic of Korea
Funder
Chung-Ang University
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol502951v
Reference23 articles.
1. β-Chlorovinyl Ketones
2. Stereoselective Synthesis of β-Chlorovinyl Ketones and Arenes by the Catalytic Addition of Acid Chlorides to Alkynes
3. Studies on Elimination Pathways of β-Halovinyl Ketones Leading to Allenyl and Propargyl Ketones and Furans under the Action of Mild Bases
4. A Soft Vinyl Enolization Approach to α-Acylvinyl Anions: Direct Aldol/Aldol Condensation Reactions of (E)-β-Chlorovinyl Ketones
5. Ambivalent Reactivity Modes of β-Chlorovinyl Ketones: Electrophilic Lithium [3]Cumulenolates from Soft Vinyl Enolization Strategy
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