Thionyl chloride-mediated synthesis of 2-azaindolizine sulfur-bridged dimers by C-H bond direct chalcogenation of imidazo[1,5-a]pyridines

DOI: 10.1002/jccs.201900516

Source and publish data:

Journal of the Chinese Chemical Society p. 1887 - 1894 (2020)

Update date:2022-08-04

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Authors:

Kulkarni, Mahesh R.

Lad, Nitin P.

Patil, Shashikant M.

Gaikwad, Nitin D.

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Article abstract of DOI:10.1002/jccs.201900516

Thionyl chloride-mediated chalcogenation of imidazo[1,5-a]pyridine serves as a new protocol for the synthesis of rare bisimidazopyridyl sulfides. This method provides the new route to synthesis of 2-azaindolizine sulfur-bridged dimers called chalcogenide

Full text of DOI:10.1002/jccs.201900516

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