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Electrophilic fluorinating

Fluoroxytrifluoromethane, a source of electrophilic fluorine, has recently been employed by Barton et al. for the fluorination of unsaturated steroids. ... [Pg.483]

Table 3. Comparison of Electrophilic Fluorination of Aromatic Amino Acids with [ F]fluorine or [ F]acetyl Hypofluorite" [25]... Table 3. Comparison of Electrophilic Fluorination of Aromatic Amino Acids with [ F]fluorine or [ F]acetyl Hypofluorite" [25]...
There are other reagents, such as CF3OF and CH3C02F, that transfer an electrophilic fluorine to double bonds. These reactions probably involve an ion pair that collapses to an addition product. [Pg.303]

More pertinent to the interests of fluoro-organic chemists, a number of compounds bearing a single N—F bond have become useful electrophilic fluorination reagents, i.e., behaving as effective sources of F+. The structures of some of them are given below, along with the chemical shifts for the N—F fluorine substituent. [Pg.223]

Like nitrogen fluorides, compounds having an O—F bond are also very strong oxidants and, when utilized as such, are effective sources of electrophilic fluorine. Because the O—F bond is so weak, the chemistry of such compounds approaches that of F2 itself, and such chemistry can be free radical or electrophilic in nature, depending on the conditions and the reactants. [Pg.226]

There are several new methodologies based on the Julia olefination reaction. For example, 2-(benzo[t/Jthiazol-2-ylsulfonyl)-j -methoxy-i -methylacetamide 178, prepared in two steps from 2-chloro-iV-methoxy-jV-methylacetamide, reacts with a variety of aldehydes in the presence of sodium hydride to furnish the ajl-unsaturated Weinreb amides 179 <06EJOC2851>. An efficient synthesis of fluorinated olefins 182 features the Julia olefination of aldehydes or ketones with a-fluoro l,3-benzothiazol-2-yl sulfones 181, readily available from l,3-benzothiazol-2-yl sulfones 180 via electrophilic fluorination <06OL1553>. A similar strategy has been applied to the synthesis of a-fluoro acrylates 185 <06OL4457>. [Pg.258]

Additional publications from Sanford et al. describe the full exploration of palladium-catalyzed chelate-directed chlorination, bromination, and iodination of arenes using N-halosuccinimides as the terminal oxidant <06T11483>. Moreover, an electrophilic fluorination of dihalopyridine-4-carboxaldehydes was reported by Shin et al. <06JFC755>. This was accomplished via transmetalation of the bromo derivative, followed by treatment with A-fluorobenzenesulfinimide as the source of electrophilic fluorine. [Pg.320]

Electrophilic fluorinating agents, 77 847 Electrophilic quench, 72 828 Electrophilic reactions... [Pg.309]

Recently, it has been shown that the reactivity and selectivity of [ F]p2 in the electrophilic fluorination of l-DOPA can be modulated by using different acidic solvents (Scheme 7). These conditions have been exploited to produce clinically useful quantities of the regioisomer [5- F]fluoro-L-DOPA [69]. [Pg.213]

Fluoroxpergfluoroalkanes, 26 123-127 tert-butane, 26 125-126 electrophilic fluorination, 26 125 methane... [Pg.109]

One may conclude that the above-mentioned anhydrous [ F]fluorine compounds, except perhaps H[ F]F, have been abandoned, partly because of their limited potential and difficulty of preparation and also because of the success of the main three agents of today, [ F]fluoride (see Section 4), p F]fluorine gas (see Section 3.1.1) and acetyl [ F]hypofluorite (see Section 3.1.3). The advent of the first one, ([ F]fluoride), made less urgent the need for high-specific-activity electrophilic fluorine and the latter two, ([ F]fluorine gas and acetyl p F]hypo-fluorite), are able to perform practically all low-specific-activity electrophilic syntheses (see Section 3), putting a brake on the development of alternatives. [Pg.14]

Electrophilic fluorination is the process by which fluorine is delivered to an electron-donating reactant, such as an alkene, aromatic ring or carbanion, by a formal positive-fluorine reagent to form a carbon-fluorine covalent bond. These reactions are fast and have proven extremely valuable for some important fluorine-18-labelled radiopharmaceuticals. Over the years several reviews on electrophilic fluorination were written. The reader is encouraged to seek out these works for greater detail on the subject [7,68-70]. [Pg.14]

In this section the production of a number of radioactive electrophilic fluorination agents that have not already been dealt with in Section 2.6 will be discussed. [Pg.15]

Scheme 12. Mechanisms of electrophilic fluorination of a carbon-carbon double bond. Scheme 12. Mechanisms of electrophilic fluorination of a carbon-carbon double bond.
Scheme 25. The arenium ion mechanism of electrophilic fluorination of aromatic rings via fluorodehydrogenation or fluorodemetallation reactions. Scheme 25. The arenium ion mechanism of electrophilic fluorination of aromatic rings via fluorodehydrogenation or fluorodemetallation reactions.
Another example of a direct electrophilic fluorination of aromatic rings is the synthesis of the purine derivatives 8-[ F]fluoroganciclovir, 8-[ F]fluoropenciclo-vir and 8-[ F]fluoroacyclovir (Scheme 27). The radiochemical yields obtained for these compounds are low, about 1%, but no protecting group is required, allowing a one-step radiosynthesis [107]. [Pg.25]

The consistent poor regioselectivity in direct aromatic electrophilic fluorination has privileged the use of fluorodemetallation reactions. Tin clearly appears to... [Pg.25]

K. Adachi, Y. Ohira, G. Tomizawa, S. Ishihara, S. Oishi, Electrophilic fluorination with N,N -difluoro-2,2 -bipyridinium salt and elemental fluorine, J. Fluorine Chem. 120 (2003) 173-183. [Pg.258]

Erythromycins are macrolide antibiotics produced by bacterial fermentation. Fluoiination of erythromycin has been studied as a strategy to insure better stability in acidic medium and/or to achieve better bioavailability. An erythromycin, fluorinated at C-8, flurithromycin, was launched several years ago. Its preparation involves an electrophilic fluorination, with CF3OF [119] or with an N-F reagent A/-fluorobenzenesulfonimide (NFSI) [120], of the 8,9-anhydroerythromy-cin-6,9-hemiacetal or of the erythronolide A (Fig. 44). [Pg.590]

Several 2-fluoroerythromycin derivatives have also been prepared by means of electrophilic fluorination with Selectfluor of the enolate of the )S-ketoester fragment (Fig. 45) [121]. Fluorination is stereoselective and leads to the a-fluo-rine compound [122]. Two derivatives of 2-fluoroerythromycin are in clinical development HMR-3562 and HMR-3787). These compounds are promising agents for the treatment of respiratory pathogens resistant to erythromycin A (Fig. 45) [123]. [Pg.591]


See other pages where Electrophilic fluorinating is mentioned: [Pg.124]    [Pg.132]    [Pg.474]    [Pg.46]    [Pg.133]    [Pg.209]    [Pg.911]    [Pg.11]    [Pg.223]    [Pg.320]    [Pg.416]    [Pg.231]    [Pg.75]    [Pg.230]    [Pg.407]    [Pg.231]    [Pg.212]    [Pg.214]    [Pg.218]    [Pg.229]    [Pg.3]    [Pg.11]    [Pg.12]    [Pg.13]    [Pg.15]    [Pg.15]    [Pg.16]    [Pg.598]   


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Achirality electrophilic fluorinating

Acyl chlorides, electrophilic fluorination

Aldehydes electrophilic fluorination

Carbonyl compounds electrophilic fluorination

Chiral auxiliaries electrophilic fluorination

Diastereoselective synthesis electrophilic fluorination

Electrophiles asymmetric fluorination

Electrophilic Fluorination - Cesium Fluorosulfate

Electrophilic Fluorination Reactions

Electrophilic Fluorination with F-TEDA-BF4 (Selectfluor)

Electrophilic aromatic substitution fluorine

Electrophilic fluorinating agents containing N-F bonds

Electrophilic fluorinating agents, preparation

Electrophilic fluorinating reagents

Electrophilic fluorination

Electrophilic fluorination aromatic compound

Electrophilic fluorination reagents

Electrophilic fluorination reagents acetyl hypofluorite

Electrophilic fluorination reagents application

Electrophilic fluorination reagents molecular fluorine

Electrophilic fluorination reagents perchloryl fluoride

Electrophilic fluorination reagents trifluoromethyl hypofluorite

Elemental fluorine as an electrophile

Enantioselective synthesis electrophilic fluorination

Enolates asymmetric electrophilic fluorinations

Enones, a-fluorosynthesis via electrophilic fluorination

Fluorinating agents electrophilic

Fluorination electrophilic, mechanism

Fluoroxytrifluoromethane fluorination, electrophilic

Halogens electrophilic fluorinating agents

Hydrogen-transfer reactions electrophilic fluorination

Ketones electrophilic fluorination

Malonates electrophilic fluorination

Organotin electrophilic fluorination

Radiopharmaceuticals electrophilic fluorinations

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