In situ vinylindole synthesis. Diels-alder reactions with maleimides to give tetrahydrocarbazoles

Tetrahydrocarbazoles have been prepared in one-flask syntheses from indoles, ketones or aldehydes, and maleimides, with acid catalysis. The reactions involve a condensation of the indole with the ketone or aldehyde, followed by an in situ trapping of the vinylindole in a Diels-Alder addition with a maleimide. Isomerization of the double bond into the indole nucleus gave the tetrahydrocarbazoles which were isolated ( 6, 9 , and 10 ). Variation of the indole, carbonyl compound, and maleimide has been explored. The predominant stereochemistry of the tetrahydro ring in the products is all-cis, although a second stereoisomer has been isolated. Two regioisomers were generated from all unsymmetrical 2-alkanones, except 2-butanone, which gave the single isomer 9a . Aromatization of tetrahydrocarbazoles 6 to carbazoles 7 was accomplished with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone.     

Laser Based Techniques for Ultra Trace Isotope Production, Spectroscopy and Detection

A variety of research activities in the field of fundamental and applied nuclear physics has evolved in the last years using resonantly tuned radiation from powerful lasers. The technique of resonance ionization spectroscopy has delivered outstanding results and found broad acceptance in the last years as a particularly efficient and highly selective method for rare and exotic radioisotope studies. It is used for production, spectroscopy and detection of these species and provides complete isobaric, high isotopic and even some isomeric selection, which altogether is needed for on-line investigation of short lived species far off stability as well as for ultra trace determination. Good overall efficiency pushes the experimental limits of detection in elemental trace analysis down to below 10⁶ atoms per sample, and additionally isotopic selectivity as high as 3 × 10¹² has been demonstrated. The widespread potential of resonance ionization techniques is discussed, focusing on the experimental arrangements for applications in selective on-line isotope production, spectroscopy of rare radioisotopes and ultra trace determination of radiotoxic isotopes like ²³⁸Pu to ²⁴⁴Pu, ^135,137Cs, ^89,90Sr or ⁴¹Ca in environmental, technical and biomedical samples.     

Naturally occuring lactones and lactames—V: Halogenated β-keto esters as starting materials for the synthesis of tetronic acids

In an effort to improve and simplify the synthetic route to tetronic acids 15 differently substituted β-keto esters were investigated as potential starting materials. The β-keto esters were brominated and cyclised with 2·5 N KOH as cyclising agent. Tetronic acid and seven derivatives including the naturally occuring carolinic acid were obtained. In a number of cases products arising from a Favorskii rearrangment were isolated. The NMR spectroscopic data are discussed.