Synthesis of regio- and stereospecifically deuterium labelled 2-benzylindanes

Kuck D (1984)
Zeitschrift für Naturforschung B, Journal of Chemical Sciences 39(3): 369-374.

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Journal Article | Published | English
Abstract
2-Benzylindenes are hydrogenated to 2-benzylindanes using tris-(triphenylphosphine)-rhodium(I)-chloride in benzene by a strict cis-1,2 addition of hydrogen to the double bond. Thus, stereo- and region-specific deuterium labelling at the five-membered ring of various 2-benzylindanes has been carried out. The high selectivity of deuterium incorporation is shown independently by 1H NMR and mass (MIKE) spectrometry of selected 2-benzylindanes.
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Kuck D. Synthesis of regio- and stereospecifically deuterium labelled 2-benzylindanes. Zeitschrift für Naturforschung B, Journal of Chemical Sciences. 1984;39(3):369-374.
Kuck, D. (1984). Synthesis of regio- and stereospecifically deuterium labelled 2-benzylindanes. Zeitschrift für Naturforschung B, Journal of Chemical Sciences, 39(3), 369-374.
Kuck, D. (1984). Synthesis of regio- and stereospecifically deuterium labelled 2-benzylindanes. Zeitschrift für Naturforschung B, Journal of Chemical Sciences 39, 369-374.
Kuck, D., 1984. Synthesis of regio- and stereospecifically deuterium labelled 2-benzylindanes. Zeitschrift für Naturforschung B, Journal of Chemical Sciences, 39(3), p 369-374.
D. Kuck, “Synthesis of regio- and stereospecifically deuterium labelled 2-benzylindanes”, Zeitschrift für Naturforschung B, Journal of Chemical Sciences, vol. 39, 1984, pp. 369-374.
Kuck, D.: Synthesis of regio- and stereospecifically deuterium labelled 2-benzylindanes. Zeitschrift für Naturforschung B, Journal of Chemical Sciences. 39, 369-374 (1984).
Kuck, Dietmar. “Synthesis of regio- and stereospecifically deuterium labelled 2-benzylindanes”. Zeitschrift für Naturforschung B, Journal of Chemical Sciences 39.3 (1984): 369-374.
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