Publications: Difference between revisions

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86. "A Facile One–step Synthesis of 2,4–Adamantanedione," Bobek, M. M.; Brinker, U. H. [https://doi.org/10.1080/00397919908085947 ''Synthetic Commun''. '''1999''', ''29'', 3221 – 3225].
86. "A Facile One–step Synthesis of 2,4–Adamantanedione," Bobek, M. M.; Brinker, U. H. [https://doi.org/10.1080/00397919908085947 ''Synthetic Commun''. '''1999''', ''29'', 3221 – 3225].


85. ''Carbene Rearrangements LI:'' "Competitive Intramolecular Reactions of ''n''–Alkenyl- and ''n''–Alkyl–substituted Cyclopropylidenes: An Insertion Reaction into Non–activated C–H Bonds,” Brinker, U. H.; Miebach, T. [http://pubs.acs.org/doi/abs/10.1021/jo990972t ''J. Org. Chem''. '''1999''', ''64'', 8000 – 8003].
85. ''Carbene Rearrangements LI:'' "Competitive Intramolecular Reactions of ''n''–Alkenyl– and ''n''–Alkyl–substituted Cyclopropylidenes: An Insertion Reaction into Non–activated C–H Bonds,” Brinker, U. H.; Miebach, T. [http://pubs.acs.org/doi/abs/10.1021/jo990972t ''J. Org. Chem''. '''1999''', ''64'', 8000 – 8003].


84. ''Carbene Rearrangements L:'' "1–Bromobicyclo[1.1.0]butane as an Easily Obtainable C4–Building Block: A Novel Route to Cyclobutanone," Weber, J.; Haslinger, U.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo980190k ''J. Org. Chem''. '''1999''', ''64'', 6085 – 6086].
84. ''Carbene Rearrangements L:'' "1–Bromobicyclo[1.1.0]butane as an Easily Obtainable C4–Building Block: A Novel Route to Cyclobutanone," Weber, J.; Haslinger, U.; Brinker, U. H. [http://pubs.acs.org/doi/abs/10.1021/jo980190k ''J. Org. Chem''. '''1999''', ''64'', 6085 – 6086].

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