Allyl iodide (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Allyl iodide" in English language version.

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  • Bertleff, Werner (2000). "Carbonylation". Ullmann's Encyclopedia of Industrial Chemistry. pp. 9, 14–15. doi:10.1002/14356007.a05_217. ISBN 978-3527306732. When unsaturated amines are carbonylated in the presence of Co2(CO)8, N-alkyl pyrrolidinones are obtained. Carbonylation of allyl halides in the presence of primary amines and a rhodium compound affords the same products....If allyl derivatives are carbonylated in the presence of acetylene by means of Ni(CO)4 and water or methanol at 20 °C, the acetylene adds onto the allyl halide and 2-cis-5-dienoic acids or esters or sorbic acid esters are obtained.
  • Wollweber, Hartmund (2000). "Hypnotics". Ullmann's Encyclopedia of Industrial Chemistry. p. 521. doi:10.1002/14356007.a13_533. ISBN 978-3527306732. Disubstitution of barbituric acids at the 5-position is only possible with highly reactive halides, such as allyl halides.
  • Behr, Arno (2000). "Organometallic Compounds and Homogeneous Catalysis". Ullmann's Encyclopedia of Industrial Chemistry. p. 10. doi:10.1002/14356007.a18_215. ISBN 978-3527306732. Halogen-containing allyl complexes can often be prepared simply from reactions of allyl halides with metal compounds.
  • Datta, Rasek Lal (March 1914). "The Preparation of Allyl Iodide". Journal of the American Chemical Society. 36 (5): 1005–1007. doi:10.1021/ja02182a023. Retrieved 15 December 2013.

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