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

Allyl radical     prop-1-ene

Synonyms: prop-2-enyl, AC1L3VXF, prop-1-en-3-yl, AR-1H6794, AC1Q2A5W, ...
 
 
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 propane

 

Biological context of propane

  • Sinigrin (2-propenyl glucosinolate) was found to be relatively innocuous to all of the organisms tested but its hydrolysis to yield isothiocyanates, thiocyanates and nitriles resulted in inhibition of growth [5].
 

Anatomical context of propane

 

Associations of propane with other chemical compounds

  • By comparison of the transient visible absorption and the 1315 nm I atom absorption from 266 nm photolysis of vinyl iodide and allyl iodide, the absorption cross sections at 404 nm of vinyl radical ((2.9 +/- 0.4) x 10(-19) cm(2)) and allyl radical ((3.6 +/- 0.8) x 10(-19) cm(2)) were derived [4].
 

Gene context of propane

  • For the allyl radical, CC3 adiabatic excitation energies differ from experiment by less than 0.02 eV, while for the (2)Sigma(+) state of CH, significant errors of more than 0.4 eV remain [7].
 

Analytical, diagnostic and therapeutic context of propane

  • Electronic absorption spectra in the 210-250 nm region, were reported for the allyl radical in the vapor phase and subsequent reactions have been investigated by kinetic spectroscopy and gas-liquid chromatography [8].

References

  1. High enantioselectivity in rhodium-catalyzed allylic alkylation of 1-substituted 2-propenyl acetates. Hayashi, T., Okada, A., Suzuka, T., Kawatsura, M. Org. Lett. (2003) [Pubmed]
  2. Modulatory influence of sodium 2-propenyl thiosulfate from garlic on cyclooxygenase activity in canine platelets: possible mechanism for the anti-aggregatory effect. Chang, H.S., Yamato, O., Yamasaki, M., Maede, Y. Prostaglandins Leukot. Essent. Fatty Acids (2005) [Pubmed]
  3. Novel strategies for the solid phase synthesis of substituted indolines and indoles. Nicolaou, K.C., Roecker, A.J., Hughes, R., van Summeren, R., Pfefferkorn, J.A., Winssinger, N. Bioorg. Med. Chem. (2003) [Pubmed]
  4. Ultraviolet photochemistry of trichlorovinylsilane and allyltrichlorosilane: vinyl radical (HCCH2) and allyl radical (H2CCHCH2) production in 193 nm photolysis. DeSain, J.D., Jusinski, L.E., Taatjes, C.A. Physical chemistry chemical physics : PCCP. (2006) [Pubmed]
  5. The effects of glucosinolates and their hydrolysis products on microbial growth. Brabban, A.D., Edwards, C. J. Appl. Bacteriol. (1995) [Pubmed]
  6. Isolation and identification of sodium 2-propenyl thiosulfate from boiled garlic (Allium sativum) that oxidizes canine erythrocytes. Yamato, O., Sugiyama, Y., Matsuura, H., Lee, K.W., Goto, K., Hossain, M.A., Maede, Y., Yoshihara, T. Biosci. Biotechnol. Biochem. (2003) [Pubmed]
  7. Coupled cluster methods including triple excitations for excited states of radicals. Smith, C.E., King, R.A., Crawford, T.D. The Journal of chemical physics. (2005) [Pubmed]
  8. High resolution electronic absorption and extinction coefficients of the allyl radical. Bayrakçeken, F., Aktaş, S., Unlügedik, A., Karaaslan, I. Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. (2003) [Pubmed]
 
WikiGenes - Universities