The metal catalyzed reactions of diazo compounds have been broadly used in organic synthesis. The resulting metal–carbenoid intermediates are capable of undergoing a range of unconventional reactions, and due to their high energy, they are ideal for initiating cascade sequences leading to the rapid generation of structural complexity. This tutorial review will give an overview of the most versatile reactions of donor/acceptor carbenoids, an exciting class of intermediates capable of highly selective reactions. This will include cyclopropanation, [4 + 3] cycloaddition, and C–H functionalization methodologies. The application of this chemistry to the synthesis of a range of natural products will be described.
A review, with 46 references, describing the most versatile reactions of donor/acceptor-carbenoids, including cyclopropanation, [4 + 3] cycloaddition and C–H functionalisation, and the application of these reactions to natural product synthesis.
A review, with 46 references, looking at the synthesis of natural products starting from donor/acceptor-carbenoids.