TY - JOUR
A1 - Huisgen, R.
A1 - Christl, Manfred
T1 - 1,3-Dipolare Cycloadditionen der Knallsäure
N2 - No abstract available
Y1 - 1967
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30227
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Huisgen, R.
T1 - Alte und neue Cycloadditionen der Nitriloxide
N2 - No abstract available
Y1 - 1968
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30237
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Reich, H. J.
A1 - Roberts, J. D.
T1 - Nuclear Magnetic Resonance Spectroscopy. Carbon-13 Chemical Shifts of Methylcyclopentanes, Cyclopentanols, and Cyclopentyl Acetates
N2 - No abstract available
KW - Organische Chemie
Y1 - 1971
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57862
ER -
TY - JOUR
A1 - Bast, K.
A1 - Christl, Manfred
A1 - Huisgen, R.
A1 - Mack, W.
T1 - Additionen der Nitriloxide an CN-Mehrfachbindungen
N2 - No abstract available
KW - Organische Chemie
Y1 - 1972
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57879
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Roberts, J. D.
T1 - Nuclear Magnetic Resonance Spectroscopy : Carbon-13 Chemical Shifts of Small Peptides as a Function of pH
N2 - No abstract available
KW - Organische Chemie
Y1 - 1972
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57885
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Roberts, John D.
T1 - Carbon-13 Nuclear Magnetic Resonance Spectroscopy : Conformational Analysis of Methyl-Substituted Cycloheptanes, Cycloheptanols, and Cycloheptanones
N2 - The 130 chemical shifts were determined of the carbons in 12 cycloheptanes, 21 cycloheptanols, and 8 cycloheptanones. In some cyc1oheptanols and cyc1oheptanones, the assignments have been obtained unambiguously by the synthesis of deuterated derivatives and the use of paramagnetic-shift reagents. Substituent effects for the different types of groups have been calculated. The most informative data about the cyc10heptane conformations were provided by the relatively well understood I' effects. The results are generally in,good agreement with predictions based on the twist-chair form, which has been predicted by Hendrickson to be the most stable conformation. Pairs of cis-trans isomers are found to have rather characteristic differences in their 130 spectra. This fact was used to assign the resonances found for cis-trans mixtures of methyl-substituted cyc1oheptanols to specific isomers.
Y1 - 1972
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-41663
ER -
TY - JOUR
A1 - Bast, K.
A1 - Christl, Manfred
A1 - Huisgen, R.
A1 - Mack, W.
A1 - Sustmann, R.
T1 - Additionen des Benzonitriloxids an olefinische und acetylenische Dipolarophile
N2 - No abstract available
KW - Organische Chemie
Y1 - 1973
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57905
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Warren, J. D.
A1 - Hawkins, B. L.
A1 - Roberts, J. D.
T1 - \(^{13}\)C and \(^{15}\)N Nuclear Magnetic Resonance Spectroscopy of Nitrile Oxides and Related Reaction Products : Unexpected \(^{13}\)C and \(^{15}\)N Nuclear Magnetic Resonance Parameters of 2,4,6-Trimethylbenzonitrile Oxide
N2 - No abstract available
KW - Organische Chemie
Y1 - 1973
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57894
ER -
TY - JOUR
A1 - Bast, K.
A1 - Christl, Manfred
A1 - Huisgen, R.
A1 - Sustmann, R.
T1 - Zur Anlagerung des Benzonitriloxids an α,β-ungesättigte Carbonsäureester
N2 - No abstract available
KW - Organische Chemie
Y1 - 1973
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57912
ER -
TY - JOUR
A1 - Huisgen, R.
A1 - Christl, Manfred
T1 - Reaktionen der Knallsäure mit ungesättigten Verbindungen
N2 - No abstract available
KW - Organische Chemie
Y1 - 1973
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57927
ER -
TY - JOUR
A1 - Bast, K.
A1 - Christl, Manfred
A1 - Huisgen, R.
A1 - Mack, W.
T1 - Relative Dipolarophilen-Aktivitäten bei Cycloadditionen des Benzonitriloxids
N2 - No abstract available
KW - Organische Chemie
Y1 - 1973
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57935
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Huisgen, R.
T1 - Orientierungsphänomene bei der Cycloaddition aliphatischer und aromatischer Nitriloxide an α,β-ungesättigte Carbonester
N2 - No abstract available
KW - Organische Chemie
Y1 - 1973
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57942
ER -
TY - JOUR
A1 - Brüntrup, Gisela
A1 - Christl, Manfred
T1 - Darstellung und Thermolyse der Hexamethyldewarbenzol-Cycloaddukte aromatischer Nitriloxide und des Diphenylnitrilimins
N2 - No abstract available
Y1 - 1973
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30257
ER -
TY - JOUR
A1 - Christl, Manfred
T1 - Cycloaddition an Benzvalen
N2 - No abstract available
Y1 - 1973
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30217
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Brüntrup, Gisela
T1 - Diimine Reduction and Ozonolysis of Benzvalene
N2 - Via reduction of benzvalene (1) with diirnine tricyclo[3.1.0.02•6]hexane is obtained in good yield. The procedure renders 3, which has already been synthesized by Lemal and Shim, accessible much easier and in larger quantities. IH and 13C n.m.r. spectroscopic data are discussed. Both the thermal and the AgBF4-catalyzed rearrangernent of 3 yield 1,3-cyclohexadiene (8). - The ozonolysis of 1 with subsequent LiAIH4-reduction results in cis-I,3- bis(hydroxyrnethyl)cyclobutane (13a).
N2 - Durch Reduktion von Benzvalen (1) mit Diimin wird das Tricyc1o[3.1.0.02•6]hexan (3) in guter Ausbeute erhalten. Das Verfahren macht das bereits von Lemal und Shim dargestellte 3 erheblich leichter und in größeren Mengen zugänglich. IH- und 13C-NMR-spektroskopische Daten werden diskutiert. Sowohl die thermische als auch die AgBF4-katalysierte Umlagerung von 3 führt zu 1,3-Cyclohexadien (8). - Die Ozonolyse von 1 mit anschließender LiAlH4-Reduktion ergibt das cis-l,3-Bis(hydroxymethyl)cyclobutan (13a).
KW - Organische Chemie
Y1 - 1974
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57953
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Brüntrup, Gisela
T1 - Neue Isomere des Cycloheptatriens: Tricyclo[4.1.0.0^(2,7)]hept-3-en und Tetracyclo[4.1.0.0^(2,4).0^(3,5)]heptan
N2 - No abstract available
Y1 - 1974
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-41488
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Heinemann, U.
A1 - Kristof, W.
T1 - Thermal Rearrangement of Some Endo-Endo'-Bridged Bicyclo[1.1.0]butanes
N2 - No abstract available
KW - Organische Chemie
Y1 - 1975
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57967
ER -
TY - JOUR
A1 - Christl, Manfred
T1 - \(^{13}\)-NMR-Spektren von Bicyclo[n.1.0]kohlenwasserstoffen
N2 - No abstract available
KW - Organische Chemie
Y1 - 1975
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57977
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Lechner, M.
T1 - Zur intramolekularen Wechselwirkung von Cyclopropylidenen mit dem Bicyclo[1.1.0]butansystem
N2 - No abstract available
Y1 - 1975
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-41509
ER -
TY - JOUR
A1 - Christl, Manfred
T1 - Carbon-13 Chemical Shifts and 13C-15N Coupling Constants of 3,4-Dihydroisoquinoline-15N, its 15N-Oxide and their Conjugate Acids
N2 - No abstract available
Y1 - 1975
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30071
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Freitag, G.
T1 - Das Tricyclo[4.1.0.0\(^{2,7}\)]heptenyl-Kation, ein neues Isomer des Tropylium-Ions
N2 - No abstract available
KW - Organische Chemie
Y1 - 1976
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57985
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Lüddecke, H.-J.
A1 - Nagyrevi-Neppel, A.
A1 - Freitag, G.
T1 - Einige Diels-Alder-Additionen des Benzvalens
N2 - No abstract available
KW - Organische Chemie
Y1 - 1977
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-57992
ER -
TY - JOUR
A1 - Volz, H.
A1 - Shin, J.-H.
A1 - Prinzbach, H.
A1 - Babsch, H.
A1 - Christl, Manfred
T1 - Stability of Tricyclo[4.1.0.0\(^{2,7}\)]heptenyl-Cations
N2 - No abstract available
KW - Organische Chemie
Y1 - 1978
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58001
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Freitag, G.
A1 - Brüntrup, G.
T1 - Der Aufbau des Tetracyclo[4.1.0.0\(^{2,4}\).0\(^{3,5}\)]heptan-Systems durch Addition halogensubstituierter Carbene an Benzvalen
N2 - No abstract available
KW - Organische Chemie
Y1 - 1978
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58019
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Freitag, G.
A1 - Brüntrup, G.
T1 - Tricyclo[4.1.0.0\(^{2,7}\)]hept-3-ene durch Umlagerung von 7-endo-Brom- und 7-endo-Chlortetracyclo[4.1.0.0\(^{2,4}\).0\(^{3,5}\)]heptanen
N2 - No abstract available
KW - Organische Chemie
Y1 - 1978
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58029
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Buchner, Wolfgang
T1 - 13C-NMR-Spektren von Tetracyclo[4.1.0.02,4.03,5]heptanen, Tetracyclo[5.1.0.02,4.03,5]octanen und Tricyclo[4.1.0.02,7]hept-3-enen. Ungewöhnliche beta- und gamma-Substituenteneffekte
N2 - No abstract available
Y1 - 1978
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30087
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Herbert, R.
T1 - Unusual Carbon Shielding Effects of Cyclopropanes and Double Bonds in Strained Bicyclo[3.1.0]hexanes and Cyclopentenes
N2 - Carbon-13 shieldings and one-bond \(^{13}\)C-H coupling constants of bicydo[2.1.1]hexane, bicydo[2.l.l]hex- 2-ene, tricydo[3.1.1.0\(^{2.4}\)]heptane and benzvalene are presented and compared. to the data of related. compounds. H a bicydo[3.1.0]hexane system is part of a rigid skeleton, the cydopropane ring exerts spedfk: 'Y substituent eflects of two ldnds. In the case of the bicyclobexane boat form an upfield shift of the C-3 signal is observed and in tbe esse of the chair form a downfield shift of 15-20 ppm. Compared to the corresponding cydopentanes the double bond in strained cydopentenes causes downfield shifts of the C-4 absorption. 1bis eftect increases witb increasing strain, reaching 8 45.9 ppm maximum in benzvalene. Hence it is tbe only known bicydo[l.l.O]butane baving 8 reversed order of carbon shieldings. The downfield shifts are e:xplained by means of simple orbital interaction schemes.
KW - Organische Chemie
Y1 - 1979
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58038
ER -
TY - JOUR
A1 - Herbert, R.
A1 - Christl, Manfred
T1 - Bicyclo[2.1.1]hexane aus Tricyclo[3.1.0.0\(^{2,6}\)]hexanen
N2 - No abstract available
KW - Organische Chemie
Y1 - 1979
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58042
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Herbert, R.
T1 - Der Einfluß anellierter Ringe auf die \(^{13}\)C-NMR-chemischen Verschiebungen von Tricyclo[3.1.0.0\(^{2,6}\)]hexan- und Bicyclo[2.1.1]hexan-Derivaten
N2 - No abstract available
KW - Organische Chemie
Y1 - 1979
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58058
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Leininger, Hartmut
T1 - 7-Azatetracyclo[4.1.0.02,4.03,5]heptan - ein neues Valenzisomeres des Azepins
N2 - No abstract available
Y1 - 1979
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30034
ER -
TY - JOUR
A1 - Leininger, H.
A1 - Christl, Manfred
T1 - Oxidationsreaktionen am Benzvalen: Ozonolyse, cis-Hydroxylierung, Epoxidation und Singulettsauerstoff-Addition
N2 - No abstract available
KW - Organische Chemie
Y1 - 1980
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58088
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Lang, R.
A1 - Herbert, R.
A1 - Freitag, G.
T1 - Zusammenhang zwischen Orbitalcharakter und Reaktionsprodukt bei der Umsetzung von Benzvalen und Homobenzvalen mit Thiophenol
N2 - No abstract available
KW - Organische Chemie
Y1 - 1980
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58065
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Lang, R.
A1 - Lechner, M.
T1 - Tetra- und pentacyclische Tricyclo[4.1.0.0\(^{2,7}\)]hept-3-en-Derivate; Abfangprodukte des Tricyclo[4.1.0.0\(^{2,7}\)]hepta-3,4-diens
N2 - No abstract available
KW - Organische Chemie
Y1 - 1980
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58078
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Brunn, E.
T1 - Tetracyclo[4.1.0.0\(^{2,4}\).0\(^{3,5}\)]heptane aus 7,8-Diazatetracyclo[4.3.0.0\(^{2,4}\).0\(^{3,5}\)]non-7-enen
N2 - No abstract available
KW - Organische Chemie
Y1 - 1981
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58094
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Lanzendörfer, Ulrike
A1 - Freund, Silke
T1 - Olefinadditionen an 2,5-Diphenyl-1,3,4-oxadiazin-6-on
N2 - No abstract available
Y1 - 1981
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-41525
N1 - Prof. Siegfried Hünig zum 60. Geburtstag gewidmet
ER -
TY - JOUR
A1 - Christl, Manfred
T1 - Benzvalen - Eigenschaften und Synthesepotential
N2 - No abstract available
Y1 - 1981
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30041
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Lechner, M.
T1 - Einige Reaktionen des 8,8-Dibromtetracyclo[5.1.0.0\(^{2,4}\).0\(^{3,5}\)]octans
N2 - No abstract available
KW - Organische Chemie
Y1 - 1982
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58108
ER -
TY - JOUR
A1 - Leininger, H.
A1 - Kemmer, P.
A1 - Beck, K.
A1 - Christl, M.
T1 - 7-Thiatetracyclo[4.1.0.0\(^{2,4}\).0\(^{3,5}\)]heptan (Benzvalensulfid) - Synthese und Reaktionen
N2 - No abstract available
KW - Organische Chemie
Y1 - 1982
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58113
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Lang, R.
T1 - Tricyclo[5.1.0.0\(^{2,8}\)]octa-3,5-diene (Octavalene)
N2 - No abstract available
KW - Organische Chemie
Y1 - 1982
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58124
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Leininger, Hartmut
A1 - Brunn, Erich
T1 - Carbon-13 Nuclear Magnetic Resonance Spectra of 7-Heterotetracyclo[4.1.0.02,4.03,5]heptanes. Annelation Effects of Aziridine, Oxirane, and Thiirane Rings. Unusual gamma and delta Substituent Effects
N2 - No abstract available
Y1 - 1982
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30010
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 - 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 - Christl, Manfred
A1 - Lanzendörfer, F.
A1 - Peters, K.
A1 - Peters, E.-M.
A1 - Schnering, H. G. von
T1 - Die Reaktionen von 2,5-Diaryl-1,3,4-oxadiazin-6-onen mit trans-Cycloocten, cis,trans-Cyclooctadien und Cyclopropenen
N2 - The transient [4+2]-cycloadducts from the title components eliminate nitrogen to form a 3,4-dihydro-2-pyrone derivative, a tricyclic cyclobutanone derivative and 2,5-dihydrooxepin-2-one derivatives, respectively.
KW - Organische Chemie
Y1 - 1983
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58156
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Leininger, Hartmut
A1 - Mattauch, Brigitte
T1 - The 13C NMR Spectra of Some Tricyclo[2.2.0.02,6]hexane Derivatives : Unexpected High Field Absorptions Due to Additive gamma-anti Subsituent Effects
N2 - By means of the BC NMR spectra of tricyclo{2.2.0~rfJ6Jhexane and thirteen of its derivatives the effects of substituents in endo-3- and endo-5-positions on the HC chemical shifts have been determined. The y-anti effects are at least as Jarge as in monosubstituted cyc1obutanes, where the shielding values of second-row hetero substituents exceed those in unstrained systems by far, and higher-row and carbon substituents still cause substantial upfield shifts. In the title system the y-anti effect of a substituent in the endo-3- and endo-5-position are operative additively, and thus shift the absorption of C-J upfieJd by a maximum of 27 ppm with respect to the unsubstituted hydrocarbon.
Y1 - 1983
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-41620
SN - x
ER -
TY - JOUR
A1 - Lanzendörfer, Franz
A1 - Christl, Manfred
T1 - 3,4-Bismethylentricyclo[3.1.0.02,6]hexan - Synthese und Diels-Alder-Addition an Tetracyanethylen
N2 - No abstract available
Y1 - 1983
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30263
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Leininger, Hartmut
A1 - Brückner, Dieter
T1 - On the Nature of the Bicyclo [3.2.1]octa-3,6-dien-2-yl Anion: A 13C NMR spectroscopic study
N2 - No abstract available
Y1 - 1983
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30060
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Lang, R.
A1 - Reimann, W.
A1 - Irngartinger, H.
T1 - Darstellung und Röntgenstrukturanalyse des Diels-Alder-Addukts von 4-Phenyl-4H-1,2,4-triazol-3,5-dion an Octavalen
N2 - No abstract available
KW - Organische Chemie
Y1 - 1984
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58162
ER -
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 - Christl, Manfred
A1 - Brunn, Erich
A1 - Lanzendorfer, Franz
T1 - Reactions of Benzvalene with Tetracyanoethylene, 2,3-Dichloro-5,6-dicyano-rho-benzoquinone, Chlorosulfonyl Isocyanate, and Sulfur Dioxide. Evidence for Concerted 1,4-Cycloadditions to a Vinylcyclopropane System
N2 - No abstract available
Y1 - 1984
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-30052
ER -
TY - JOUR
A1 - Christl, Manfred
A1 - Freund, S.
T1 - Substituierte Benzobenzvalene und Diazabenzobenzvalene - Synthesen aus Diels-Alder-Addukten des Benzvalens und NMR-Spektroskopie
N2 - No abstract available
KW - Organische Chemie
Y1 - 1985
U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:bvb:20-opus-58183
ER -