2-Pyranyl esters, tetrahydro

Protection of carboxyl groups as tetrahydro-2-pyranyl esters... [Pg.78]

Of more direct interest is the preparation of 3-ethylquinuclidine by this method (Prelog, Sogtaric and Gustak (1940)). Ethyl tetrahydropyranyl ketone (X R = tetrahydropyranyl in X to XIV) was condensed wiA ethyl brpmoacetate (XI) to give the hydroxy-acid ester (XII) which was dehydrated by potassium acid sulphate at 90° to ethyl 3-(tetrahydro-pyranyl-4)-pentenate (XIII) and this hydrogenated to tie corresponding... [Pg.456]

The hydroxyl group was usually protected, because cyanohydrins have tendency to racemization or even decomposition. Vinyl ethers or acetal and acid catalysts furnish acetals [62]. Trialkylsilyl chlorides and imidazole are used to give silyl ethers [63]. Commonly used protective groups are silyl ether, ester, methoxy isopropyl (MIP) ether, and tetrahydro-pyranyl ether. ( -Protected cyanohydrins are tolerant to a wider range of cyanide/nitrile transformations and are utilized widely in the synthesis of compounds of synthetic relevance in organic chemistry. [Pg.114]

Magnesium-sodiumJ alcohol Tri(methylols) from malonic acid esters via benzyloxymethylmalonic acid esters Protection of alcohol groups as tetrahydro-2-pyranyl ethers... [Pg.456]

Big Chemical Encyclopedia