Multicomponent reactions (MCRs) involving isocyanates are a potent and elegant approach to obtain compounds of interest from the agrochemical and pharmaceutical industries, both in the prototypes discovery, to turn possible the synthesis of structural diversity in a faster and practical way, as well as for the optimization of routes synthetic drugs. Although still little explored, recent work has demonstrated the possibility of developing effective catalytic systems for the asymmetric addition of ±-substituted isocyanoacetates to Michael acceptors to obtain isocyanides containing tertiary and quaternary stereocenters. The MCRs relevance in the synthesis of compounds using green chemistry, as well as the importance of the development of asymmetric methods to obtain enantiomerically pure compounds should be emphasized. In this work we propose the employment scope expansion of asymmetric MCRs with the study of induction in products of reactions that use chiral isonitriles obtained by Michael addition reaction, using organocatalysis.
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