Electron-withdrawing groups heteroatom

Substituted isoxazoles, pyrazoles and isothiazoles can exist in two tautomeric forms (139, 140 Z = 0, N or S Table 37). Amino compounds exist as such as expected, and so do the hydroxy compounds under most conditions. The stability of the OH forms of these 3-hydroxy-l,2-azoles is explained by the weakened basicity of the ring nitrogen atom in the 2-position due to the adjacent heteroatom at the 1-position and the oxygen substituent at the 3-position. This concentration of electron-withdrawing groups near the basic nitrogen atom causes these compounds to exist mainly in the OH form. 

The incorporation of heteroatoms can result in stereoelectronic effects that have a pronounced effect on conformation and, ultimately, on reactivity. It is known from numerous examples in carbohydrate chemistry that pyranose sugars substituted with an electron-withdrawing group such as halogen or alkoxy at C-1 are often more stable when the substituent has an axial, rather than an equatorial, orientation. This tendency is not limited to carbohydrates but carries over to simpler ring systems such as 2-substituted tetrahydropyrans. The phenomenon is known as the anomeric ect, because it involves a substituent at the anomeric position in carbohydrate pyranose rings. Scheme 3.1 lists... 

This review concerns in the first part the works published during the last three years on the synthesis and reactivity of stabilized ylides C-substituted by electron-withdrawing groups (COR, CO2R, CN, etc.). The second part deals with the works published in the same period on the chemistry of phosphorus ylides mainly C-substituted by heteroatoms of groups 1-16 (metals, metalloids and nonmetal elements Li, Ba, Ca, Ti, Zr, Nb, Mo, Re, Fe, Ru, Rh, Pd, Pt, Au, Zn, Hg, B, Si, Sn, N, P, As, Sb, O, S, Te). 

This section deals with alkylidene complexes L M=CR2 and vinylidene complexes LnM=(C)n,=CR2 in which the metal-bound carbon atom bears only hydrogen, alkyl, or aryl groups, but neither heteroatoms (halogen, nitrogen, oxygen, or sulfur) nor electron-withdrawing groups. Dimetallacyclopropanes and ketene complexes will not be discussed. 

DFT calculations have been used to follow the formation of iminium ions from secondary amines and acrolein.56 Energy barriers in the process can be lowered by incorporation of a heteroatom (N or O) in the a-position of the amine, or an electron-withdrawing group (carbonyl or thiocarbonyl) in the -position. 

Heteroatoms or functional groups can either increase or diminish the rate of autoxidation of alkyl groups. Haloalkanes and alkanes substituted with electron-withdrawing groups are usually more resistant toward homolytic C-H bond cleav-... 

A different mechanism operates in the direct a-heteroatom functionalization of carbonyl compounds when chiral bases such as cinchona alkaloids are used as the catalysts. The mechanism is outlined in Scheme 2.26 for quinine as the chiral catalyst quinine can deprotonate the substrate when the substituents have strong electron-withdrawing groups. This reaction generates a nucleophile in a chiral pocket (see Fig. 2.6), and the electrophile can thus approach only one of the enantiotopic faces. 

Lithiation by deprotonation of a C-H bond takes place at a reasonable rate only if the organolithium product displays two features intramolecular coordination of the electron-deficient lithium atom to a heteroatom (hydrocarbons are extremely slow to lithiate under most conditions, even at aromatic or vinylic sites) and stabilisation of the electron-rich C-Li bond by a nearby empty orbital or electron-withdrawing group. These two factors controlling lithiation are of varying importance according to the reaction in question, and the balance between them is a recurring theme of this chapter. 

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