Tetrahydropyranylation of alcohols and phenols, acetylation of aldehydes and N-Boc protection of amines are efficiently catalyzed by melamine trisulfonic acid (MTSA). All reactions were performed at room temperature in good to high yields.

a variety of alcohols readily add to 3,4-dihydro-2h-pyran under solvent free conditions in the presence of catalytic amount of acidic ionic liquid [et3n(ch2)4so3h][ots] to afford the corresponding tetrahydropyranyl ethers in good to excellent yields at room temperature. the use of this procedure allows easy separation of the desired products from ionic liquid and recycling the ionic liquid. som...

A simple and mild method for tetrahydropyranylation of alcohols is reported at room temperature using a catalytic amount of 3-methylimidazolinium hydrogensulfate([Hmim]HSO4) as a green, efficient and reusable catalyst. Using solvent-free conditions, non-toxic and inexpensive materials, modest and clean work-up, short reaction times and high yields of the products are the advantages o...

Catalytic amount of Ce(IV) as ceric triethylammonium nitrate (CTEAN) in dichloromethane or acetone can bring about an efficient tetrahydropyranylation of different types of alcohols to afford the corrsesponding tetrahydropyranyl ethers in high yields. Deportection of tetrahydropyranyl ethers can also be achieved efficiently in the presence of this catalyst in methanol.