SEARCH Articles Figures Tables 2- ethyl ethers, to protect 2- ethyl ethers, to protect alcohols 2-Methoxyethoxymethyl ethers to protect alcohols 2-Methoxyethoxymethyl ethers to protect phenols 4- phenyldiphenylmethyl ethers, to protect alcohols 9-Anthryl ethers, to protect alcohols Acid To ether Acid anhydrides hydrogenation to ethers Addition of hydrogen halide to unsaturated alcohols, ethers, carbonyl compounds, and nitriles Alcohols to ethers Alkene To ether Alkyl Halides to Dialkyl Ethers Azaacetals to ethers Bis ethers, to protect diols Bis methyl ethers, to protect Bis methyl ethers, to protect alcohols Boron trifluoride, with dimethyl ether and epichlorohydrin to give trimethyloxonium tetrafluoroborate Conversion esters to fluoro ethers Conversion of Alcohols to Ethers Conversion to enol ethers Conversion to ether Crown Ethers. From Serendipity to Design Crown ethers 1,2-additions to carbonyl compounds Cycloaddition to vinyl ether Diethyl ether hydrogen bonding to water Dimethyl ether, with boron trifluoride diethyl etherate and epichlorohydrin to give trimethyloxonium Diols to cyclic ethers Enol ethers to protect carbonyl groups Epichlorohydrin reaction with boron trifluoride etherate to form triethyloxonium fluoborate Ethanol conversion to diethyl ether Ethers cleavage to fluoroalkanes Ethers to acetals Ethers to carbonium ions Ethers to esters Ethers to esters and lactones Ethers to lactones Ethers to protect alcohols Ethers to protect phenols Ethers, allyl isomerization to propargyl ether Ethers, chlorofluorocyclopropyl to a-fluoroacrolein Ethers, epoxy to oxazolines Ethyl ethers, to protect phenols Hydrogenolysis, of phenolic ethers to aromatics Hydrolysis, amide to acid ether Hydroxyalkenes to Brominated Cyclic Ethers Hydroxyalkenes to Cyclic Ethers Introduction to Ethers Ketals, reduction to hydroxyalkyl ethers L- ethyl ethers, to protect L- ethyl ethers, to protect alcohols Methoxymethyl ethers to protect phenols Methyllithium, with camphor tosylhydrazone to give 2-bomene ether solution Methylthiomethyl ethers to protect alcohols Methylthiomethyl ethers to protect phenols O-Nitrobenzyl ethers to protect phenols Of p-methoxybenzyl ethers, to form Of p-methoxybenzyl ethers, to form alcohols Organic chemistry Ethers to isocyanates Ortho-to-ether position Oxime ethers to amines P-Methoxybenzyl ethers to protect alcohols P-Methoxybenzyl ethers to protect phenols Phenols to ethers Polyaromatic Ethers and Thioethers Coordinated to Cyclopentadienyliron Cations Rearrangement to Silyl Enol Ethers Reduction to ethers Silyl enol ethers conversion to a-hydroxyketones by oxidation Silyl enol ethers conversion to enolates Silyl ethers to protect phenols Tetrahydropyranyl ethers to protect phenols The Oxygen of an Ether Croup Is Bonded to Two Carbon Atoms Thioacetals to ethers Triphenylsilyl ethers, to protect Triphenylsilyl ethers, to protect alcohols Two Different Heteroatom Groups Attached to CF2 Including Chloro- and Bromodifluoromethyl Ethers With persulfate, potassium hydrogenation to ethers