Relevant Developments in the Use of Three‐Component Reactions for the Total Synthesis of Natural Products. The last 15 Years
Prof. Enrique L. Larghi,
Dr. Andrea B. J. Bracca,
Dr. Sebastian O. Simonetti,
Prof. Teodoro S. Kaufman
Affiliations
Prof. Enrique L. Larghi
Instituto de Química Rosario IQUIR (CONICET-UNR) Facultad de Ciencias Bioquímicas y Farmacéuticas Universidad Nacional de Rosario (UNR) Suipacha 531 2000 Rosario Argentina
Dr. Andrea B. J. Bracca
Instituto de Química Rosario IQUIR (CONICET-UNR) Facultad de Ciencias Bioquímicas y Farmacéuticas Universidad Nacional de Rosario (UNR) Suipacha 531 2000 Rosario Argentina
Dr. Sebastian O. Simonetti
Instituto de Química Rosario IQUIR (CONICET-UNR) Facultad de Ciencias Bioquímicas y Farmacéuticas Universidad Nacional de Rosario (UNR) Suipacha 531 2000 Rosario Argentina
Prof. Teodoro S. Kaufman
Instituto de Química Rosario IQUIR (CONICET-UNR) Facultad de Ciencias Bioquímicas y Farmacéuticas Universidad Nacional de Rosario (UNR) Suipacha 531 2000 Rosario Argentina
Abstract Multicomponent reactions (MCRs) offer a highly useful and valuable strategy that can fulfill an important role in synthesizing complex polysubstituted compounds, by simplifying otherwise long sequences and increasing their efficiency. The total synthesis of selected natural products employing three‐component reactions as their common strategic MCR approach, is reviewed on a case‐by‐case basis with selected targets conquered during the last 15 years. The revision includes detailed descriptions of the selected successful sequences; relevant information on the isolation, and bioactivity of the different natural targets is also briefly provided.