Tandem Transformations via Friedel–Crafts Acylation Followed by a Ring-Expansion, Ring-Opening, and Cycloisomerization Sequence
Author:
Affiliation:
1. Center for Metareceptome Research, College of Pharmacy, Chung-Ang University, 84 Heukseok-ro, Dongjak, Seoul 06974, Republic of Korea
Funder
National Research Foundation of Korea
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b03881
Reference21 articles.
1. β-Chlorovinyl Ketones
2. Stereoselective Synthesis of β-Chlorovinyl Ketones and Arenes by the Catalytic Addition of Acid Chlorides to Alkynes
3. Synthesis of Cyclic Thioethers through Tandem C(sp3)−S and C(sp2)−S Bond Formations from α,β‘-Dichloro Vinyl Ketones
4. A Facile Access to 4-Substituted-2-naphthols via a Tandem Friedel–Crafts Reaction: A β-Chlorovinyl Ketone Pathway
5. Unified Approach to (Thio)chromenones via One-Pot Friedel–Crafts Acylation/Cyclization: Distinctive Mechanistic Pathways of β-Chlorovinyl Ketones
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