Some alcohols (eg. methanol, ethanol, propanols) and some phenols are good soluble in water.But because of their greatest acidity than alcohols, phenols form salts with strong bases good soluble in water and insoluble in many organic solvents. So, alcohols can be separated from water solution ...
di- or polyglycidyl ethers of polyhydric aliphatic alcohols such as 1,4-butanediol, or polyalkylene glycols such as polypropylene glycols; di- or polyglycidyl ethers of cycloaliphatic polyols such as 2,2-bis(4-hydroxycyclohexyl)propane; di- or polyglycidyl ethers of polyhydric phenols such as reso...
(such as pinoresinol or 1-acetoxypinoresinol), other secoiridoids (such as ligstroside and its demethylated derivative), phenolic alcohols (HT), and several flavonoids and flavonols, cinnamic acid derivatives (such as verbascoside), and phenolic acids can also be found [26,47,48,69,73,...
Amongst the alkylation, diazoesters, alcohols, and alkenes are used as alkylating sources, and the reactions are mostly established with expensive and deleterious 4d and 5d transition metal catalysts (Scheme 1a) [13–21]. However, the employment of challenging alkyl halides as coupling partners in...
R5in formula IV can be a branched or a linear alkyl radical; however, alkanesulfonic acids or alkanesulfonates having linear (=straight-chain) alkyl radicals are of particular practical importance, these being distinguished by their good degradability from an ecological aspect, in addition to their...