Journal of the American Chemical Society · 1996 · 60 citations · 15 references
Natural SciencesChemistryOrganic ChemistryOrganometallic ChemistrySpectroscopyHeterocyclic ChemistryInfrared SpectroscopyReaction MechanismsHeterocyclic ReactivityInfrared Absorption SpectroscopyPyridine ChemistryStructure-reactivity RelationshipsTemperature Effects On Electronic Spectra
Ketenes 7, 14, and 17 have been generated in pyridine matrices and observed by infrared spectroscopy to react with pyridine at temperatures between 15 and 50 K to form ketene−pyridine ylides 12, 15, and 18 . Azaheterocyclic ketenes 20, 23, and 26 dimerize or tetramerize at ca . 50 K, whereby one ketene molecule acts as a nucleophile toward the other, forming a transient ketene−imine ylide.
15
α-Oxoketenes - Preparation and Chemistry
Curt Wentrup, Werner Heilmayer, G. Kollenz · Synthesis · 1994 · 133 citations
Natural Sciences, Chemistry, Natural Product Biosynthesis +12
Fernando P. Cossío, Ana Arrieta, Begoña Lecea et al. · Journal of the American Chemical Society · 1994 · 105 citations