Publication | Closed Access
Functionalized Nanodiamonds Part 3: Thiolation of Tertiary/Bridgehead Alcohols
74
Citations
27
References
2006
Year
Diamond-like CarbonMedicinal ChemistryChemical EngineeringDiamondoid ThiolsEngineeringNovel OrganocatalystsNanomaterialsNatural SciencesOrganic ChemistryTertiary/bridgehead AlcoholsProspective Nanoelectronic MaterialsChemistryHeterocycle ChemistryNatural Product SynthesisEnantioselective SynthesisAcetic Acid
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.
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