Affiliation:
1. Institute of Chemistry, Saint Petersburg State University
2. Immanuel Kant Baltic Federal University
Abstract
AbstractThe use of readily available 1-aryl-3-arylidenepyrrolidine-2,5-diones in high yielding direct diazo-transfer reactions and subsequent involvement of the resulting diazo compounds in RhII-catalyzed O–H, S–H, and N–H insertion reactions delivered 4-substituted 1-aryl-3-arylidenepyrrolidine-2,5-diones of defined regiochemistry and geometrical configuration. These products are intended to be studied as Michael acceptors capable of inhibiting thioredoxin reductase, a promising cancer target.
Funder
Russian Foundation for Basic Research
Subject
Organic Chemistry,Catalysis
Cited by
18 articles.
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