Zwitterionic intermediates generated from the addition of nonprotic nucleophiles to activated acetylenes are intercepted with various third components constituting novel multicomponent organic transformations. Catalytic amounts of an organic base like pyridine were found to trigger reactions between an electrophilic acetylene and a variety of electrophiles. The reactions proceed through dipolar intermediates and show high stereoselectivity. © 2005 IUPAC.
CITATION STYLE
Nair, V., Menon, R. S., & Sreekumar, V. (2005). Multicomponent reactions based on nucleophilic carbenes and their applications in organic synthesis. In Pure and Applied Chemistry (Vol. 77, pp. 1191–1198). https://doi.org/10.1351/pac200577071191
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