TY - JOUR A1 - Christl, Manfred A1 - Leininger, H. A1 - Kemmer, P. T1 - Über das cis-Glycol und das Epoxid des Benzvalens N2 - No abstract available KW - Organische Chemie Y1 - 1984 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58174 ER - TY - JOUR A1 - Leininger, H. A1 - Christl, Manfred A1 - Wendisch, D. T1 - Über die Oxidation von Benzvalen mit Singulett-Sauerstoff zum Bicyclo[1.1.0]butan-endo,endo-2,4-dicarbaldehyd N2 - No abstract available KW - Organische Chemie Y1 - 1983 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58142 ER - TY - JOUR A1 - Leininger, H. A1 - Lanzendörfer, F. A1 - Christl, Manfred T1 - Über die Reduktion des Benzvalenozonids zum cis-1,3-Cyclobutandimethanol mit LiAlH\(_4\) N2 - No abstract available KW - Organische Chemie Y1 - 1983 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58130 ER - TY - JOUR A1 - Christl, Manfred A1 - Hegmann, J. A1 - Reuchlein, H. A1 - Peters, K. A1 - Peters, E.-M. A1 - Schnering, H. G. von T1 - Überbrückte neungliedrige α,β-ungesättigte Enollactone - Synthese aus 5-Phenyl-1,3,4-oxadiazin-6-on-2-carbonsäure-methylester und Konfigurationsanalyse N2 - The γ-oxoketenes, which are formed from oxadiazinone Ja and strained cyclopentene der1vat1ves, are shown to undergo a pericyclic ring enlargement to give the title compounds 2a, 2b, and 5. In the case of 5, two configurations, one having a cis and the other a trans Iactone functionality, are in equilibrium. KW - Organische Chemie Y1 - 1987 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58395 ER - TY - JOUR A1 - Hegmann, J. A1 - Ditterich, E. A1 - Hüttner, G. A1 - Christl, Manfred A1 - Peters, K. A1 - Peters, E.-M. A1 - Schnering, H. G. von T1 - δ-Chlor-δ-lactone aus γ-Oxoketenen N2 - No abstract available KW - Organische Chemie KW - 1 KW - 3 KW - 4-0xadiazine-2-carboxylate KW - methyl 6-oxo-5-phenyl- KW - Diels-Alder reactions KW - Ketenes KW - y-oxo- KW - δ-Lactones KW - δ-chloro- KW - β-Lactones Y1 - 1992 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58649 ER -