Publications: Difference between revisions

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==1970 – 1979==
==1970 – 1979==


12. ''Carbene Rearrangements III:'' " Carbene Rearrangements of 2–Vinylcyclobutylidene," Brinker, U. H.; König, L. [http://pubs.acs.org/doi/pdf/10.1021/ja00510a055 ''J. Am. Chem. Soc.'' '''1979''', ''101'', 4738 – 4739].
12. ''Carbene Rearrangements III:'' "Carbene Rearrangements of 2–Vinylcyclobutylidene," Brinker, U. H.; König, L. [http://pubs.acs.org/doi/pdf/10.1021/ja00510a055 ''J. Am. Chem. Soc.'' '''1979''', ''101'', 4738 – 4739].


11. ''Carbene Rearrangements II:'' "Carbene–Carbene Rearrangements of ''cis''– and ''trans''–2–(1,3–Butadienyl)cyclopropylidene," Brinker, U. H.; Fleischhauer, I. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197903961 ''Angew. Chem.'' '''1979''', ''91'', 424 – 425]  [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197903961''Angew. Chem., Int. Ed. Engl.'' '''1979''', ''18'', 396 – 397].
11. ''Carbene Rearrangements II:'' "Carbene–Carbene Rearrangements of ''cis''– and ''trans''–2–(1,3–Butadienyl)cyclopropylidene," Brinker, U. H.; Fleischhauer, I. [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197903961 ''Angew. Chem.'' '''1979''', ''91'', 424 – 425]  [http://onlinelibrary.wiley.com/doi/abs/10.1002/anie.197903961''Angew. Chem., Int. Ed. Engl.'' '''1979''', ''18'', 396 – 397].
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6. "A Facile Photochemically Induced Arylcarbene – Aromatic Carbene Rearrangement in Solution," Brinker, U. H.; Jones, W. M. [https://doi.org/10.1016/S0040-4039(00)77915-9 ''Tetrahedron Lett.'' '''1976''', ''17'', 577 – 580].
6. "A Facile Photochemically Induced Arylcarbene – Aromatic Carbene Rearrangement in Solution," Brinker, U. H.; Jones, W. M. [https://doi.org/10.1016/S0040-4039(00)77915-9 ''Tetrahedron Lett.'' '''1976''', ''17'', 577 – 580].


5. "2,3–Dichloro–5,6–dicyano–''p''–benzoquinone (DDQ); A New Inexpensive Recovery by Anodic Oxidation of 2,3–Dichloro–5,6–dicyano–''p''–hydroquinone (DDH)," Brinker, U. H.; Tyner III, M.; Jones, W. M. [https://www.researchgate.net/publication/235706637_23-Dichloro-56-dicyano-p-benzoquinone_DDQ_A_New_Inexpensive_Recovery_by_Anodic_Oxidation_of_23-Dichloro-56-dicyano-p-hydroquinone_DDH ''Synthesis'' '''1975''', 671 – 672].
5. "2,3–Dichloro–5,6–dicyano–''p''–benzoquinone (DDQ); A New Inexpensive Recovery by Anodic Oxidation of 2,3–Dichloro–5,6–dicyano–''p''–hydroquinone (DDH)," Brinker, U. H.; Tyner III, M.; Jones, W. M. [https://www.researchgate.net/publication/235706637_23-Dichloro-56-dicyano-p-benzoquinone_DDQ_A_New_Inexpensive_Recovery_by_Anodic_Oxidation_of_23-Dichloro-56-dicyano-p-hydroquinone_DDH ''Synthesis'' '''1975''', 671].


4. "Potential Homoaromatic Compounds with 10 and 14π Electron Systems," Brinker, U. H., Doctoral Dissertation (Dr. rer. nat.), University of Cologne, Federal Republic of Germany, 1973, self-published (in German).
4. "Potential Homoaromatic Compounds with 10 and 14π Electron Systems," Brinker, U. H., Doctoral Dissertation (Dr. rer. nat.), University of Cologne, Federal Republic of Germany, 1973, self-published (in German).