Oxide function

Remote Oxidation (functionalization) Comprehensive Organic Synthesis 1991, 7, 39. [Pg.22]

Three oxidative reactions of benzene with Pd(OAc)2 via reactive rr-aryl-Pd complexes are known. The insertion of alkenes and elimination afford arylalk-enes. The oxidative functionalization of alkenes with aromatics is treated in Section 2.8. Two other reactions, oxidative homocoupling[324,325] and the acetoxylation[326], are treated in this section. The palladation of aromatic compounds is possible only with Pd(OAc)2. No reaction takes place with PdCl2. [Pg.74]

The N-oxide function has proved useful for the activation of the pyridine ring, directed toward both nucleophilic and electrophilic attack (see Amine oxides). However, pyridine N-oxides have not been used widely ia iadustrial practice, because reactions involving them almost iavariably produce at least some isomeric by-products, a dding to the cost of purification of the desired isomer. Frequently, attack takes place first at the O-substituent, with subsequent rearrangement iato the ring. For example, 3-picoline N-oxide [1003-73-2] (40) reacts with acetic anhydride to give a mixture of pyridone products ia equal amounts, 5-methyl-2-pyridone [1003-68-5] and 3-methyl-2-pyridone [1003-56-1] (11). [Pg.328]

A very useful procedure for introducing a cyano group into a pyridazine ring is the Reissert-type reaction of the A/-oxide with cyanide ion in the presence of an acyl halide or dimethyl sulfate. The cyano group is introduced into the a-position with respect to the A-oxide function of the starting compound. The yields are, however, generally poor. In this way, 6-cyanopyridazines (111) can be obtained from the corresponding pyridazine 1-oxides (Scheme 33). [Pg.24]

Nitropyridazines are reduced catalytically either over platinum, Raney nickel or palladium-charcoal catalyst. When an N-oxide function is present, palladium-charcoal in neutral solution is used in order to obtain the corresponding amino N-oxide. On the other hand, when hydrogenation is carried out in aqueous or alcoholic hydrochloric acid and palladium-charcoal or Raney nickel are used for the reduction of the nitro group, deoxygenation of the N- oxide takes place simultaneously. Halonitropyridazines and their N- oxides are reduced, dehalogenated and deoxygenated to aminopyridazines or to aminopyridazine N- oxides under analogous conditions. [Pg.34]

Lithium aluminum deuteride reduction of the 2a,3a-oxide function has been carried out with a number of different 5a-steroids (227). ° The isotopic purity of the resulting 2 -d,-3a-ols (228) is usually 96-100%. By mild oxidation, under Jones conditions, these alcohols can be converted into stereospecifically labeled monodeuterio ketones (229) ° of high isotopic purity. (For an alternate preparation of certain a-monodeuterio ketones, see section VI-B.)... [Pg.204]

UV irradiation of 3-aminopyrido[4,3-e]-1,2,4-triazine 1-oxides 7 or 1,2,4-triazine 4-oxides 8 leads to deoxygenation, i.e., loss of the 7V-oxide function resulting in the corresponding 3-aminopyrido[4,3-e]-1,2,4-triazines 9 and 1,2,4-triazines 10 (76ACH327, 76LA153). At the same time, UV irradiation of the 1,2,4-triazine 4-oxides unsubstituted at the 5 position proceeds as a ring contraction to form triazoles 11 (76LA153). [Pg.267]

The mechanism for the conversion of the A -oxide (94) to the o-methylaminophenylquinoxaline (96) involves an initial protonation of the A -oxide function. This enhances the electrophilic reactivity of the a-carbon atom which then effects an intramolecular electrophilic substitution at an ortho position of the anilide ring to give the spiro-lactam (98). Hydrolytic ring cleavage of (98) gives the acid (99), which undergoes ready dehydration and decarboxylation to (96), the availability of the cyclic transition state facilitating these processes. ... [Pg.236]

Neither the oxide nor the amidine function are in fact required for activity. Treatment of the oxime, 7, with chloro-acetyl chloride in the presence of sodium hydroxide proceeds directly to the benzodiazepine ring system (14)(the hydroxyl ion presumably fulfills a role analogous to methylamine in the above rearrangement). Reduction of the N-oxide function of 14 leads to diazepam (15). ... [Pg.365]

Compound 16, the projected precursor of 15, could conceivably be assembled from bishomoallylic alcohol 17 via a pathway that features the oxidative functionalization of the A20,21 double bond with participation by the C-17 secondary hydroxyl. Compound 17 is an attractive retrosynthetic precursor for compound 16 because the A20-21 double bond, which could permit the introduction of the adjacent C-20 and C-21 stereocenters in 16, provides a convenient opportunity for significant molecular simplification. Thus, retrosynthetic cleavage of the A20 21 double bond in 17 furnishes compounds 18 and 19 as potential building blocks. The convergent union of the latter two compounds through a Wittig reaction would be expected to afford 17 stereoselectively. [Pg.193]

Although beyond the scope of the present discussion, another key realization that has shaped the definition of click chemistry in recent years was that while olefins, through their selective oxidative functionalization, provide convenient access to reactive modules, the assembly of these energetic blocks into the final structures is best achieved through cydoaddition reactions involving carbon-het-eroatom bond formation, such as [l,3]-dipolar cydoadditions and hetero-Diels-Al-der reactions. The copper(i)-catalyzed cydoaddition of azides and terminal alkynes [5] is arguably the most powerful and reliable way to date to stitch a broad variety... [Pg.445]

Besides current development of new catalysts and related functional materials, oxidation tools have always played an important role in their synthesis, activation, and functionalization. After a separate discussion per technique we have rationalized our literature findings (Table 6.2) as five principal oxidative functions with many proven applications. [Pg.136]

Heterocyclic N-oxides such as pyridine, quinoline, or isoquinoline N-oxides can be converted into a mixture of 2- and some 4-cyanopyridines, 2- or 4-cyanoquino-lines, or 1-cyanoisoquinolines, in 40-70% yield, in a Reissert-Henze reaction, by activation of the N-oxide function by O-acylation [1] or O-alkylation [2, 3] followed by treatment with aqueous alkali metal cyanide in H2O or dioxane. [Pg.147]

HMDSO 7 [39]. With 20/DIPEA sulfoxide 1233 affords 76% of 1235 [40]. Analogous silylation of the S-oxide function in 1237 with the O-silylketene acetal 1214 and subsequent cyclization with ZnCl2 or Znl2 affords 1238, a precursor of thie-namycin [41-43] (Scheme 8.16). [Pg.196]

Klemm and coworkers studied the spectra of several thienopyridine sulfones (72-78) and found that it is possible to distinguish by mass spectrometry between a sulfone function and a combination of two sulfoxide or JV-oxide functions in the same molecule . For instance, compound 77 forms 78 losing the 7V-oxygen atom, since except for the molecular ion their mass spectra are very similar. Compound 78 rearranges prior to fragmentation to the two possible cyclic sulfinates (80 and 81), which then fragment further by losing SO and CNO, respectively. [Pg.145]

Ozone diffuses readily into amorphous region of the polyethylene (32) and oxidation probably occurs much deeper in the solid sample. Ozone also attacks the crystalline part of polyethylene but it has a slow initiation stage followed by more rapid oxidation (13). Because ozone does not diffuse into the crystalline regions (13.32). oxidation is restricted to the surface. The resulting oxidized functional groups on the crystalline regions will remain at the surface, whereas those formed in the amorphous region can diffuse into the bulk. [Pg.193]

Regulation of the total oxidation of reductants (HC, CxIIvO.) by 02, taking into account the difference of temperature between their mild oxidation by NOz and their total oxidation by dioxygen. This point requires the choice of a total oxidation function, but not too much active. [Pg.171]

The powdered oxidant functions as an explosive when mixed with finely divided metals, organic materials or sulfur, which increase the shock-sensitivity up to that of picric acid [1]. The hazardous properties of such mixtures increase as the particle size of the oxidant salt decreases [2],... [Pg.1368]

An explosion in flour-bleaching operations was attributed to violent decomposition of the basic nitrate [1], which is an impact-, friction- and heat-sensitive explosive [2]. The instability is associated with the presence of reducant and oxidant functions in the same molecule. The previous formulation as tin(II) nitrate oxide is revised to that above. [Pg.1684]

In Section 4.2 an analysis based on bond lengths and dipole moments was presented showing that structures I and II contribute about equally to the actual structure. Nitrous oxide functions as an oxidizing agent that can react explosively with H2,... [Pg.489]

Several secondary metabolites are dithiolanes, as for instance the allelochem-icals found in the tropical weed, Sphenoclea zeylanica. Zeylanoxide A is present in two stereoisomeric forms depending on whether the chirality at sulfur is (R) or (5) the latter form is 44 (Scheme 15). Zeylanoxides B are similar but in these cases the oxide function is on the sulfur at the 2 position. These molecules inhibited root growth in rice seedlings as well as the germination of letuce seeds.95... [Pg.694]

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