- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Klassifikation
-
Chemie
- Ereignis
-
Veröffentlichung
- (wo)
-
Würzburg
- (wer)
-
Universität Würzburg
- (wann)
-
2010
- Urheber
-
Christl, Manfred
- URN
-
urn:nbn:de:bvb:20-opus-41677
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:50 MEZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Christl, Manfred
- Universität Würzburg
Entstanden
- 2010
Ähnliche Objekte (12)
Carbon-13 Chemical Shifts and 13C-15N Coupling Constants of 3,4-Dihydroisoquinoline-15N, its 15N-Oxide and their Conjugate Acids
Cycloaddition an Benzvalen
13C-NMR-Spektren von Bicyclo[n.1.0]kohlenwasserstoffen
Benzvalen - Eigenschaften und Synthesepotential
Photocycloadditions of Benzvalene
Tricyclo[3.1.1.02,6]hexandion (the Valen of o-Benzochinons), Bicyclo[2.1.1]hexan-2,3-dion and Valene of a Chinoxalins, of Phenazins and of a Benzophenazine
Diimine Reduction and Ozonolysis of Benzvalene
Nuclear Magnetic Resonance Spectroscopy : Carbon-13 Chemical Shifts of Small Peptides as a Function of pH
Generation and Interception of 1-Oxa-3,4-cyclohexadiene
Generation and interception of 1-OXA-2,3-Cyclohexadiene and 1,2,4-Cyclohexatriene
Carbon-13 Nuclear Magnetic Resonance Spectroscopy : Conformational Analysis of Methyl-Substituted Cycloheptanes, Cycloheptanols, and Cycloheptanones
Unusual Carbon Shielding Effects of Cyclopropanes and Double Bonds in Strained Bicyclo[3.1.0]hexanes and Cyclopentenes
Carbon-13 Chemical Shifts and 13C-15N Coupling Constants of 3,4-Dihydroisoquinoline-15N, its 15N-Oxide and their Conjugate Acids
Cycloaddition an Benzvalen
13C-NMR-Spektren von Bicyclo[n.1.0]kohlenwasserstoffen
Benzvalen - Eigenschaften und Synthesepotential
Photocycloadditions of Benzvalene
Tricyclo[3.1.1.02,6]hexandion (the Valen of o-Benzochinons), Bicyclo[2.1.1]hexan-2,3-dion and Valene of a Chinoxalins, of Phenazins and of a Benzophenazine
Diimine Reduction and Ozonolysis of Benzvalene
Nuclear Magnetic Resonance Spectroscopy : Carbon-13 Chemical Shifts of Small Peptides as a Function of pH
Generation and Interception of 1-Oxa-3,4-cyclohexadiene
Generation and interception of 1-OXA-2,3-Cyclohexadiene and 1,2,4-Cyclohexatriene
Carbon-13 Nuclear Magnetic Resonance Spectroscopy : Conformational Analysis of Methyl-Substituted Cycloheptanes, Cycloheptanols, and Cycloheptanones
Unusual Carbon Shielding Effects of Cyclopropanes and Double Bonds in Strained Bicyclo[3.1.0]hexanes and Cyclopentenes
Carbon-13 Chemical Shifts and 13C-15N Coupling Constants of 3,4-Dihydroisoquinoline-15N, its 15N-Oxide and their Conjugate Acids
Cycloaddition an Benzvalen
13C-NMR-Spektren von Bicyclo[n.1.0]kohlenwasserstoffen
Benzvalen - Eigenschaften und Synthesepotential
Photocycloadditions of Benzvalene
Tricyclo[3.1.1.02,6]hexandion (the Valen of o-Benzochinons), Bicyclo[2.1.1]hexan-2,3-dion and Valene of a Chinoxalins, of Phenazins and of a Benzophenazine
Diimine Reduction and Ozonolysis of Benzvalene
Nuclear Magnetic Resonance Spectroscopy : Carbon-13 Chemical Shifts of Small Peptides as a Function of pH
Generation and Interception of 1-Oxa-3,4-cyclohexadiene
Generation and interception of 1-OXA-2,3-Cyclohexadiene and 1,2,4-Cyclohexatriene
Carbon-13 Nuclear Magnetic Resonance Spectroscopy : Conformational Analysis of Methyl-Substituted Cycloheptanes, Cycloheptanols, and Cycloheptanones