Answers are grounded in this paper and cite their sources.
This review summarizes advancements in guanidine-based cycloaddition reactions, highlighting trends in methodology.
Guanidines are structurally unique, highly basic, nitrogen-containing organic compounds with strong hydrogen-bonding ability and biological activity, providing valuable functionality in medicinal chemistry, organocatalysis, and materials science. Among modern strategies for assembling guanidine-containing molecules, cycloaddition reactions have emerged as powerful tools due to their efficiency, stereoselectivity, and ability to rapidly build molecular complexity. Recent innovations have expanded cycloaddition methodologies for generating guanidine functionalities, incorporating guanidine-containing substrates, and using guanidine-based catalysts. This review summarizes these advances and highlights the current trends in guanidine-related cycloaddition chemistry.
No takes yet. Share an insight, caveat, or question.
Štrbac et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: