Functionalized Nanodiamonds Part 3: Thiolation of Tertiary/Bridgehead Alcohols
Organic Letters2006Vol. 8(9), pp. 1767–1770
Citations Over TimeTop 10% of 2006 papers
Boryslav A. Tkachenko, Natalie A. Fokina, Lesya V. Chernish, Jeremy Dahl, Shenggao Liu, Robert M. K. Carlson, Andrey A. Fokin, Peter R. Schreiner
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.
Related Papers
- → Functionalized Nanodiamonds Part 3: Thiolation of Tertiary/Bridgehead Alcohols(2006)74 cited
- → Tunable synthesis of chalcophosphinic amides and tertiary phosphinates using tert-butyl N,N-dialkylperoxyamidate(2021)3 cited
- → Ruthenium-catalyzed Formation of Tertiary Amines from Nitriles and Alcohols(2011)21 cited
- → The esterification of tertiary alcohols with boric acid(1952)5 cited
- → A novel method for synthesis of unsymmetrical secondary and tertiary amines from reactions of alcohols with amines by utilizing aminophosphonium salts(1975)16 cited