Journalartikel
Autorenliste: Tkachenko, BA; Fokina, NA; Chernish, LV; Dahl, JEP; Carlson, RMK; Fokin, AA; Schreiner, PR
Jahr der Veröffentlichung: 2006
Seiten: 1767-1770
Zeitschrift: Organic Letters
Bandnummer: 8
Heftnummer: 9
ISSN: 1523-7060
DOI Link: https://doi.org/10.1021/ol053136g
Verlag: 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.
Zitierstile
Harvard-Zitierstil: 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-Zitierstil: 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
