Hydroxamic acids, cyclic reactions

The following discussion of hydroxamic acids includes saturated systems, e.g., 2, compounds such as 3, derived from aromatic systems, 7V-hydroxyimides such as 7V-hydroxyglutarimide (78), and certain of their derivatives including thiohydroxamic acids. Naturally occurring cyclic hydroxamic acids are discussed to show the range of structural types that has been found, hut macrocyclic polyhydroxamic acids are mentioned very briefly, because several comprehensive reviews of these compounds are already available. The main purpose of this review is to summarize the methods available for the synthesis of cyclic hydroxamic acids, to outline their characteristic reactions, and to present some useful physical data. Their synthesis and some biological properties have previously been reviewed by Coutts. ... 

Because of the great range of structures containing cyclic hydroxamic acid functions it is difficult to give a concise summary of the available synthetic methods. Nevertheless, the vast majority of published syntheses depend on condensation reactions involving only familiar processes of acylation or alkylation of hydroxylamine derivatives. The principles of such syntheses are outlined in a number of typical examples in Section III, A but no attempt has been made to cover all reported cases. 

A variety of condensation processes can lead to cyclic hydroxamic acids. These involve either the condensation of two molecules or the intramolecular cyclization of a single compound. In some cases, a primary hydroxamic acid function is already present and formation of a cyclic compound can arise by suitable reaction on nitrogen. These processes will be dealt with first. 

Several reactions are particularly applicable to the synthesis of cyclic hydroxamic acids as they involve some kind of ring expansion. Some are quite general reactions which are of high preparative utility, whereas others exist as fairly isolated examples which have not as yet been generalized. 

Cyclic hydroxamic acids and V-hydroxyimides are sufficiently acidic to be (9-methylated with diazomethane, although caution is necessary because complex secondary reactions may occur. N-Hydroxyisatin (105) reacted with diazomethane in acetone to give the products of ring expansion and further methylation (131, R = H or CH3). The benzalphthalimidine system (132) could not be methylated satisfactorily with diazomethane, but the V-methoxy compound was readil3 obtained by alkylation with methyl iodide and potassium carbonate in acetone. In the pyridine series, 1-benzyl-oxy and l-allyloxy-2-pyridones were formed by thermal isomeriza-tion of the corresponding 2-alkyloxypyridine V-oxides at 100°. 

Two derivatives of a cyclosilyl ether 148 have been synthesized by a German team <1994TL4335>. The enolizable cyclic hydroxamic acid 147 when treated with 2equiv of lithium diisopropylamide followed by reaction with di-fert-butyldichlorosilane in toluene yielded the stable [l,3,4,2]dioxazasilolo[5,4-c][l,4]oxazine derivative 148. 

The literature contains several references to reductive cyclizations producing cyclic hydroxamic acids like those described above, though not in solid-phase chemistry.43-47 We showed that this reaction competes well with lactam formation. The relative extent of these two reaction pathways is highly dependent on the presence and the nature of other heteroatoms and substituents around the ring system as well as on the conditions used to effect the reduction. 

The cyclohexene 121, which was readily accessible from the Diels-Alder reaction of methyl hexa-3,5-dienoate and 3,4-methylenedioxy-(3-nitrostyrene (108), served as the starting point for another formal total synthesis of ( )-lycorine (1) (Scheme 11) (113). In the event dissolving metal reduction of 121 with zinc followed by reduction of the intermediate cyclic hydroxamic acid with lithium diethoxyaluminum hydride provided the secondary amine 122. Transformation of 122 to the tetracyclic lactam 123 was achieved by sequential treatment with ethyl chloroformate and Bischler-Napieralski cyclization of the resulting carbamate with phosphorus oxychloride. Since attempts to effect cleanly the direct allylic oxidation of 123 to provide an intermediate suitable for subsequent elaboration to ( )-lycorine (1) were unsuccessful, a stepwise protocol was devised. Namely, addition of phenylselenyl bromide to 123 in acetic acid followed by hydrolysis of the intermediate acetates gave a mixture of two hydroxy se-lenides. Oxidative elimination of phenylselenous acid from the minor product afforded the allylic alcohol 124, whereas the major hydroxy selenide was resistant to oxidation and elimination. When 124 was treated with a small amount of acetic anhydride and sulfuric acid in acetic acid, the main product was the rearranged acetate 67, which had been previously converted to ( )-lycorine (108). 

Atkinson, J., Morand, P., Arnason, J. T., Niemeyer, H. M. and Bravo, H. R. 1991. Analogues of the cyclic hydroxamic acid 2,4-dihydroxy-2H-1,4-benzoxazin-3-one decomposition to benzoxazolinones and reaction with -mercaptoethanol. J. Org. Chem. 56, 1788-1800... 

A new synthesis of ( )-crinane (13) (Scheme 2) may be applicable to Amaryllidaceae alkaloids.5 Key features of the synthesis are the preparation of the acid (10) by Claisen rearrangement of the allylic acetate (9) and intramolecular ene reaction of a protected acylnitroso-enophile (11) to give the cyclic hydroxamic acid (12). 

MisceUaneous Reactions.—Details of the formation of nitrous oxide by photofragmentation of methyl nitrite have been reported.Photorearrangement is observed, however, on irradiation of the nitrites (183) derived from 6-methyl- and 4,4,6-trimethyl-cholest-5-en-3-ol to give the cyclic hydroxamic acids (184). There is ample precedent for these transformations, the likely pathway for which is outlined in Scheme 12. An alkoxyl radical (185) is also thought to be involved in the photochemicaUy induced conversion of O-nitrobenzoin (186) into benzaldehyde (187) and 2-phenylbenzo[b]furan (188). Reductive photoelimination of vicinal dinitro-groups takes place by... 

Sometimes a cathodic substitution reaction takes place during the reduction of o-substituted nitrobenzenes thus, the reduction of 2-nitrophenoxyacetic acid [52] in 2 A hydrochloric acid (50% ethanol) yielded 5-chloro-2i7-l,4-benzoxazin-3(4H)-one rather than the expected cyclic hydroxamic acid [52]. In the presence of another nucleophile Y (e.g., thiocyanate), a ring substitution with this reagent occurs. 

Alicyclic hydroxamic acids undergo several specific oxidative cleavage reactions which may be of diagnostic or preparative value. In the pyrrolidine series compounds of type 66 have been oxidized with sodium hypobromite or with periodates to give y-nitroso acids (113). Ozonolysis gives the corresponding y-nitro acids. The related cyclic aldonitrone.s are also oxidized by periodate to nitroso acids, presumably via the hydroxamic acids.This periodate fission was used in the complex degradation of J -nitrones derived from aconitine. 

Trispyrazolylborates are models for tris-histidine active sites in zinc enzymes, e.g., the matrix metalloproteinases involved in breakdown of extracellular matrices. Inhibition of these metalloproteinases may prove valuable in the treatment of, inter alios, cancer and arthritis, so efforts are being made to find appropriate ligands to block the zinc active site. The search has recently moved on from hydroxamates to hydroxypyridinones - l-hydroxy-2-pyridinone is a cyclic analogue of hydroxamic acid. As reported in Section II.B.2 earlier, hydroxypyridinones form stable five-coordinate complexes on reaction with hydrotris(3,5-phenylmethylpyrazolyl)borate zinc hydroxide. Modeling studies suggest that hydroxypyridinonate ligands should be able to access the active site in the enzyme with ease (110). 

A seemingly complex heterocycle which on close examination is in fact a latentiated derivative of a salicylic acid shows antiinflammatory activity. It might be speculated that this compound could quite easily undergo metabolic transformation to a salicylate and that this product is in fact the active drug. Condensation of acid 134 with hydroxylamine leads to the hydroxamic acid 135. Reaction of that with the ethyl acetal from 4-chlorobutyraldehyde then leads to the cyclic carbinolamine derivative 136. Treatment... 

Nitro-compounds fRNOj) are isomeric with nitrites, but their electronic structure, excited states and photochemistry are very different. There is no very low-lying (n.jt ) state, and nitroalkanes show n — 3i absorption with a maximum around 275 nm ( —201 mol - cm In cyclohexane solution, nitromethane (CH1NOi) is photoreduced to nitrosomethane(CH,NO, but nitroethane under the same conditions gives rise to a nitroso-dimer derived from the solvent CS.47). The latter process is probably initiated by cleavage of the carbon-nitrogen bond in the nitroalkane. In basic solution (when the nitroalkane is converted to a nitronate anion) irradiation can lead to efficient formation of a hydroxamic acid (S.48), and this reaction most likely proceeds through formation of an intermediate three-mem bered cyclic species. 

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