Deuteration of indole and N-methylindole by Raney nickel catalysis

DOI: 10.1002/(SICI)1099-1344(199907)42:7<709::AID-JLCR235>3.0.CO;2-2

Source and publish data:

Journal of labelled compounds and radiopharmaceuticals p. 709 - 713 (1999)

Update date:2022-08-16

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Authors:

Yau, Wai-Ming

Gawrisch, Klaus

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Article abstract of DOI:10.1002/(SICI)1099-1344(199907)42:7<709::AID-JLCR235>3.0.CO;2-2

Indole and N-methylindole have been partially or fully deuterated by Raney nickel catalyzed ¹H-²H exchange in a series of deuterated solvents. Perdeuterated indoles have been obtained in water and methanol while compounds that are preferentially deuterated at specific sites were obtained in chloroform, acetone, acetonitrile, ethanol, and isopropanol. The partially deuterated compounds are an important research tool for solid-state NMR studies on proteins.

Full text of DOI:10.1002/(SICI)1099-1344(199907)42:7<709::AID-JLCR235>3.0.CO;2-2

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