The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
Chemical Compound Review

Norbornadiene     bicyclo[2.2.1]hepta-2,5-diene

Synonyms: B33803_ALDRICH, AG-D-46575, ACMC-209sng, ANW-41402, NSC-13672, ...
 
 
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.
 

High impact information on Norbornadiene

 

Biological context of Norbornadiene

 

Associations of Norbornadiene with other chemical compounds

  • We show that the X-ray absorption spectrum of 1,4-cyclohexadiene exhibits some particular spectral structures in the discrete energy region that evidence diene through-bond orbital interaction, whereas absorption peaks are identified in the norbornadiene and norbornadienone spectra that indicate effective through-space orbital interactions [7].
  • The two former are square planar; the latter are pentacoordinated for diene = tetrafluorobenzobarrelene or norbornadiene (confirmed by X-ray diffraction), but an equilibrium of 4- and 5-coordinate isomers exists in solution for diene = 1,5-cyclooctadiene [8].
  • Carbon and oxygen near-edge X-ray absorption fine structure (NEXAFS) spectra of 1,4-cyclohexadiene, p-benzoquinone, norbornadiene, norbornadienone, and cis-cis-[4,4,2]propella-3,8-diene-11,12-dione were calculated by means of Hartree-Fock and hybrid density functional theory using the static-exchange (STEX) approximation [7].
  • 2,5-Norbornadiene (NBD) and aminoethoxyvinylglycine (AVG) reduced the basal level of ACC oxidase transcript and its enzyme activity [9].

References

  1. Light-harvesting and photoisomerization in benzophenone and norbornadiene-labeled poly(aryl ether) dendrimers via intramolecular triplet energy transfer. Chen, J., Li, S., Zhang, L., Liu, B., Han, Y., Yang, G., Li, Y. J. Am. Chem. Soc. (2005) [Pubmed]
  2. Density functional study of the retrocyclization of norbornadiene and norbornene catalyzed by Fe(+). McKee, M.L. J. Am. Chem. Soc. (2001) [Pubmed]
  3. Mutual antagonism of ethylene and jasmonic acid regulates ozone-induced spreading cell death in Arabidopsis. Tuominen, H., Overmyer, K., Keinänen, M., Kollist, H., Kangasjärvi, J. Plant J. (2004) [Pubmed]
  4. Ethylene induces epidermal cell death at the site of adventitious root emergence in rice. Mergemann, H., Sauter, M. Plant Physiol. (2000) [Pubmed]
  5. Photoinduced intramolecular electron transfer and triplet energy transfer in a steroid-linked norbornadiene-carbazole dyad. Zhang, L.P., Chen, B., Wu, L.Z., Tung, C.H., Cao, H., Tanimoto, Y. Chemistry (Weinheim an der Bergstrasse, Germany) (2003) [Pubmed]
  6. Nucleoside diphosphate kinase is a possible component of the ethylene signal transduction pathway. Novikova, G.V., Moshkov, I.E., Smith, A.R., Hall, M.A. Biochemistry Mosc. (2003) [Pubmed]
  7. Probing weak molecular orbital interactions in non-conjugated diene molecules by means of near-edge X-ray absorption spectroscopy. Felicíssimo, V.C., Cesar, A., Luo, Y., Gel'mukhanov, F., Agren, H. The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment & general theory. (2005) [Pubmed]
  8. Rhodium complexes with the chelating and binucleating ligands P(CH2CH2Py)nPh3-n (Py = 2-pyridyl; n = 1,2): structures and fluxional behavior. Alonso, M.A., Casares, J.A., Espinet, P., Soulantica, K., Charmant, J.P., Orpen, A.G. Inorganic chemistry. (2000) [Pubmed]
  9. The requirements for Ca2+, protein phosphorylation, and dephosphorylation for ethylene signal transduction in Pisum sativum L. Kwak, S.H., Lee, S.H. Plant Cell Physiol. (1997) [Pubmed]
 
WikiGenes - Universities