Journal article
Authors list: Tkachenko, BA; Fokina, NA; Chernish, LV; Dahl, JEP; Carlson, RMK; Fokin, AA; Schreiner, PR
Publication year: 2006
Pages: 1767-1770
Journal: Organic Letters
Volume number: 8
Issue number: 9
ISSN: 1523-7060
DOI Link: https://doi.org/10.1021/ol053136g
Publisher: American Chemical Society
Abstract:
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.
Citation Styles
Harvard Citation style: Tkachenko, B., Fokina, N., Chernish, L., Dahl, J., Carlson, R., Fokin, A., et al. (2006) Functionalized nanodiamonds, Part 3: Thiolation of tertiary/bridgehead alcohols, Organic Letters, 8(9), pp. 1767-1770. https://doi.org/10.1021/ol053136g
APA Citation style: Tkachenko, B., Fokina, N., Chernish, L., Dahl, J., Carlson, R., Fokin, A., & Schreiner, P. (2006). Functionalized nanodiamonds, Part 3: Thiolation of tertiary/bridgehead alcohols. Organic Letters. 8(9), 1767-1770. https://doi.org/10.1021/ol053136g
