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American Chemical Society, Organic Letters, 9(8), p. 1767-1770, 2006

DOI: 10.1021/ol053136g

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Functionalized Nanodiamonds Part 3: Thiolation of Tertiary/Bridgehead Alcohols ‖

This paper is available in a repository.
This paper is available in a repository.

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Abstract

[reaction: see text] Treatment of acyclic as well as polycyclic tertiary mono- and dihydroxy hydrocarbon derivatives with thiourea in the presence of hydrobromic and acetic acid represents a convenient one-step route to the respective tertiary thiols and dithiols. This procedure was used for the preparation of diamondoid thiols of diamantane, triamantane, [121]tetramantane, and others that are prospective nanoelectronic materials.